The Subject Of This Procedure Is The Delivery Of Medicinal Products By Dosage Form And A Unit Of Measure Included In Annex 2 Of The Positive Medicinal List (Pls). In The Technical Specification, The Medicinal Products Are Distributed In Separate Positions, Depending On Their Ats Group (Anatomo-Therapeutic Code), Inn (Internationally Non-Patent Name) And Dosage Form/ Form Of Administration (For Example: Oral, Parenteral Or Other Form). The Medicinal Products Are From Different Groups Of Medicines Needed For The Overall Treatment Of The Hospital. The Quality Of Medicinal Products Should Meet The Requirements Submitted By The Standardizing Documents Of The European Union, The Republic Of Bulgaria And The Manufacturer Or Equivalent As Follows: Directive (Eu) 2017/1572 Of The Commission Of 15 September 2017 To Supplement The European Parliament Of Products And The Gucars Of Products. Medicinal Products In Human Medicine And Ordinance No. 15 Of April 17, 2009 On The Conditions For Issuing A Production/Import Authorization And The Principles And Requirements For Good Production Practice Of All Types Of Medicinal Products, For Clinical Trial And Active Substances. These Quantities Are Estimated. The Contractor Reserves The Right Not To Declare The Estimated Estimated Quantities.
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