Phytomenadione Solution For Intramuscular Administration, 10 Mg/Ml, 1 Ml, The Supplier Is Required To Provide 1 (One) Sample Of The Product To Verify Compliance. The Item Must Be New And Unused. Products That Do Not Meet The Requirements Will Not Be Accepted. The Supplier Includes All Costs Associated With The Delivery Of The Goods: Delivery Of The Goods To The Destination. Upon Delivery, Provide Originals Or Notarized Copies Of The Factory Quality Certificate And/Or Technical Passport Of The Product Issued By The Manufacturer (Sender), Or Another Document Issued By The Manufacturer Containing Information About The Completeness Of The Product, Its Technical Characteristics, Operating Rules, Guarantees And Other Information Necessary To Determine The Quality Of The Product And Its Compliance With Regulatory And Technical Documents. If The Goods Are Of Foreign Origin, Then An Original Or A Notarized Copy Of The Relevant Certificate Of Origin Of The Goods, Issued By The Relevant Authority Of The Country Of Origin In The Prescribed Manner, Is Provided. If The Product Is Foreign-Made, Then You Need To Provide Technical Specifications In 2 Languages: Russian And Kazakh. The Shelf Life Of Medicines And Medical Devices On The Date Of Delivery By The Supplier To The Customer Is: At Least Fifty Percent Of The Indicated Shelf Life On The Packaging (If The Shelf Life Is Less Than Two Years); At Least Twelve Months From The Expiration Date Indicated On The Package (If The Expiration Date Is Two Years Or More). For Each Delivery, Provide A Registration Certificate, Certificates Of Conformity, Certificates Of Origin.
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