Deliveries Of Medicinal Products I:A. All Goods Offered, Within The Scope Of Task No. 1, Must Be Approved For Use In Medical Entities, Including Health Care Facilities, And Meet The Essential Requirements, I.E. They Must Have The Appropriate Authorization Required By The Act Of September 6, 2001, Pharmaceutical Law, For Marketing And Use In Poland, Based On An Entry In The Register Of Pharmaceuticals And Medical Materials. The Ordering Party Requires The Submission Of Documents Specified In The Act Of September 27, 2013 Amending The Pharmaceutical Law Act And Certain Other Acts And The Act On The Office For Registration Of Medicinal Products, Medical Devices And Biocidal Products Of March 18, 2011 B. Prices For Reimbursed Products Proposed In The Proceedings Cannot Be Higher Than Those Resulting From The Provisions Of Art. 9 Section 1 And 2 Of The Act Of May 12, 2011. On The Reimbursement Of Medicines, Foodstuffs For Particular Nutritional Uses And Medical Devices.C. In Justified Cases, The Ordering Party Allows Packaging With A Different Capacity (Weight) - The Demand For A Given Drug Should Then Be Calculated Appropriately And Rounded Up To The Next Full Package.
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