Request For Quotation Medicines And Other Medical Supplies. Strictly On The Terms Of The Technical Specification, Delivery In Batches Upon Request From The Customer Until 12/31/2026.

Cefekon-D 0.25 Suppositories No. 10 (From 3-12 Years). In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Prednisolone, 30 Mg 1 Ml No. 3 Adagio (Solution For Iv And Im Administration). In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage., Arpeflu 100 Mg No. 20. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Activated Carbon No. 10. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Ascorbic Acid 5% 2Ml No. 10. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Eufillin 2.4% 5Ml/10. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Arbidol 100 Mg No. 10. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Nise 1%, 20 G, Gel. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Advantan Ointment 0.1%, 15 G. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Lasix 10 Mg/Ml Amp 2 Ml. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Cerucal 10 Mg, No. 50, In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Ketonal 100 Mg 2 Ml No. 5. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Fenistil-Gel 30G. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Ketonal 50 Mg No. 25. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Hydrogen Peroxide 3% -100 Ml. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Furadonin No. 10. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Sodium Chloride 0.9% 400Ml. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Ventolin Breathing Solution 0.5%, 20Ml. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Antigrippin, No. 10. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Valerian Extract No. 50. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Through The Web Portal In The “Approval” Sheet. The Product Must Meet The Technical And Quality Characteristics. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 80% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Pancreatin No. 60. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Loperamide No. 10. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Ibuvir 250 Mg/5 Ml Syrup. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Ambrobene 7.5 Mg/Ml 100 Ml Solution. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Streptocide 300 Mg No. 10. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Chlorhexidine. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Inhalipt N Aerosol 30 Ml. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Paracetamol No. 10. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Cerucal 10 Ampoules, 2 Ml Each. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Furacillin 20 Mg No. 10 External. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., No-Spa 40 Mg, 2 Ml/10 Amp. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Hydrogen Peroxide 6%, 100 Ml. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Diclofenac-Acos 25 Mg/Ml, 3 Ml No. 10. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Syringe 2 Ml. 3 Sets In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., No-Spa (Drotaverine) 40 Mg, No. 100 Tablets. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Dexamethasone 4 Mg/1 Ml No. 5. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Furosemide 1% 2 Ml No. 10. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Cordiamine 25%, 2Ml., No. 10 Darnitsa. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Isoket Spray 1.25 Mg/Dose 15 Ml Aerosol. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Andipal No. 10. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Diphenhydramine Solution No. 10. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Anaferon For Children 300 Mg No. 20. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Levomycetin 0.5 Mg, 10 Tablets. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Dolgit 100G Cream. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Bisiprolol 2.5 No. 30. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Troxevasin Ointment 40G. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Potassium Chloride 4%, 10.0, No. 10. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Analgin 0.5 G, No. 10 Tablets. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Glucose 10%, 200 Fl. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer., Ozokerite For Medical Procedures In Kilograms. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Mukaltin 0.05 No. 10. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Pinosol Nasal Drops 10 Ml. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Nitroglycerin-Kz 0.0005 G, No. 40, Tab. Sublingual In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Lidocaine 1% 3.5 Ml. No. 5 Solution. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Sodium Chloride 0.9% 200Ml. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Cyanocobalomin Vit B12-1 Ml. No. 10. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Magnesium Sulfate R/R 250 Ml/Mg, 5/10. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Vishnevsky Liniment 40 G, Tube Delivery Of Goods Is Carried Out At The Customer’S Request In Batches Throughout The Year Until December 31, 2026, From The Date Of Submission Of The Application Within 15 Calendar Days. The Application Is Submitted Through The Web Portal In The “Approval” Sheet. The Product Must Meet The Technical And Quality Characteristics. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 80% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Tavegil 1Mg/Ml 2Ml Amp 5Pcs. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Dimexide 50 Ml. D/External Approx. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Valerian Root 50 G, Herbal Tea. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Tetracycline 1% 10G/Hl Ointment. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Platifilin 0.2%1/10. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Galazolin 0.05% 10Ml. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Yox 30 Ml, Spray. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Nimesil No. 30. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Tempalgin M500mg No. 20 Tablet. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Enap 1.25 Mg/Ml No. 5. Solution For Injection. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Adrenaline Hydrotartrate 0.18% -1 Ml., No. 10. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Angisept No. 10. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Ketorolac, Solution 1 Ml 30 Mg, No. 10. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Cough Tablets No. 10. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Analgin 50% Solution 2 Ml. No. 10. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Papaverine Hydrochloride 2% 2Ml No. 10. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Paraffin P-2 (1 Kg) In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Ammonia 10% Aqueous Solution 90Ml. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Panthenol Spray 10%. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Tylol No. 12, In Bags. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Ergoferon No. 20. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Sodium Chloride 0.9% 100Ml. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Diclofenac 1%, 30 G, Ointment. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Bromhexine 8 Mg No. 25. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Ebrantil 25 Mg. 5/5. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Captopril 25 Mg, No. 40, Tablets. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Novocaine 0.5%, 5Ml. Amp. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Calcium Chloride 10%, 5Ml, No. 5 Ampoules. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Оксалиновая Мазь 0,25% 10 Гр. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Validol 0.06 G No. 10. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Berodual Solution For Inhalation 0.25 Mg. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Sulfacyl Sodium (Albucid) 30% 10 Ml, Eye Drops. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Baralgin M No. 20 Tab. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Citramon Table No. 10. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Disol 200 Ml. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Levomekol Ointment 40 G Tube. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint., Diamond Green 1%, 20.0 Ml. In Accordance With The List Of Permits Of The First Category (Licenses), Provided For By The Law Of The Republic Of Kazakhstan “On Permits And Notifications” Dated May 16, 2014 No. 202-V Zrk (Hereinafter Referred To As The Law On Permits), The Sale Of Medicines Is A Licensed Type Of Activity. The Compliance Of The Potential Supplier And (Or) The Involved Subcontractor (Co-Contractor) With The Qualification Requirements Established By This Article Is Confirmed By Submitting To The Customer, Organizer, Single Organizer The Relevant Documents Provided For By This Law And The Rules Of Public Procurement, Or Through The Information Systems Of Government Bodies In Accordance With The Legislation Of The Republic Of Kazakhstan On Informatization. Availability Of Permission, Notification Of The Start Of Activities In Accordance With The Law. Delivery Of Goods Is Carried Out At The Request Of The Customer In Batches Throughout The Year Until December 31, 2026, From The Date Of Filing The Application Within 15 Calendar Days. The Application Is Submitted Via The Web Portal In The “Approval” Sheet. The Product Must Meet Technical And Quality Specifications. Upon Delivery Of Goods, Availability Of Accompanying Documents In Accordance With Clause 5.1 Of The Agreement. Strictly In Accordance With The Technical Specifications, As Agreed With The Customer. The Supplier Must Deliver Goods With A Remaining Shelf Life Of At Least 70% Of The Total Shelf Life. The Product Is Supplied In High-Quality Original Factory Packaging That Meets State Standards, Technical Specifications, And Other Regulatory And Technical Documentation. The Product Must Be New, The Product Packaging Must Contain The Necessary Labeling With Complete And Reliable Information About The Product, Expiration Date, Composition, Manufacturer, Etc. At The Time Of Delivery Of The Goods, All Packaging Must Be Intact, Without Traces Of Physical Or Chemical Damage. Markings Must Be Clearly Applied With Indelible Paint.