GTR 104902888

Tenders Are Invited For Vaccines - Human Rabies Vaccine (Inactivated)

ICB — International Competitive Bid Closed central europe
Tender Information
GTR Reference
104902888
Tendering Authority
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Tender No
760465-2025
Financer Name
Self-Funded
Work Title
Tenders Are Invited For Vaccines - Human Rabies Vaccine (Inactivated)
Bid Type
ICB — International Competitive Bid
Country
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Geographical Region
central europe
Political Region
European Union
Last Date of Bid Submission
16-12-2025 Closed
Work Detail
Vaccines - Human Rabies Vaccine (Inactivated). As Part Of The Sales Contract, The Applicant Acquires Human Rabies Vaccine (Inactivated), As Follows: Atc Code: J07bg01 Total Quantity: 20,000 Doses Packaging: 1 X 1-Dose Syringe If The Product Offered Is In Ampoule Packaging, 2 Needles And 1 Syringe Of The Type Recommended By The Who Must Be Included With The Vaccine. Quality Requirement: The Vaccine Must Comply With The Who Trs. 941: Recommendations For Inactivated Rabies Vaccine For Human Use Produced In Cell Substrates And Embryonated Eggs; And The Requirements Of Monograph 01/2019:0216 Of The European Pharmacopoeia. Usability: The Vaccine Must Be Usable For At Least 12 Months From The Date Of Storage. Storage Deadline: March 1, 2026, 7,000 Doses, June 1, 2026, 5,000 Doses, September 1, 2026, 5,000 Doses, December 15, 2026, 3,000 Doses. Marketing Authorization: At The Time Of Submission Of The Offer, The Vaccine Must Have The Pharmaceutical Authority (Nngyk, Or Ogyéi /Gyemszi/ Ogyi At The Time) Or Issued By The Ec On The Basis Of Regulation 726/2004/Ec Of The European Parliament And Council, Regulation 1901/2006/Ec Of The European Parliament And Council Or Regulation 1394/2007/Ec Of The European Parliament And Council. With A Valid Marketing Authorization For The Proposed Vaccine. Pharmaceutical Wholesale License: At The Time Of Submitting The Offer, The Tenderer Must Have The Eszcsm Decree 53/2004 (Vi.2.) And The 2005 Xcv. With A Valid Pharmaceutical Wholesale License According To Law, Covering The Product Group Of The Subject Of The Public Procurement. Packaging: The Recommended Vaccine Must Comply With Commission Delegated Regulation (Eu) 2016/161 Of October 2, 2015 Supplementing Directive 2001/83/Ec Of The European Parliament And Of The Council With Regard To The Definition Of Detailed Rules For Safety Elements To Be Placed On The Outer Packaging Of Medicinal Products Intended For Human Use. The Applicant Accepts Packaging In A Foreign Language, But A Patient Information Sheet In Hungarian Is Required. Delivery Means The Delivery Of The Entire Amount Of Vaccine Due At A Given Storage Date To The Place Of Delivery, And Storage Means Making The Entire Amount Of Vaccine Due At A Given Storage Date Available To The Contracting Authority In A Marketable Manner.
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