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Asia Hiv Aids Medicine Tenders

Bid on readily available Asia Hiv Aids Medicine Tenders with GlobalTenders, the biggest and best online tendering platform, since 2002. Globaltenders.com offers an unmatched database of Hiv Aids Medicine tenders from Asia, more than any other platform.

Daily, new procurement opportunities for Hiv Aids Medicine are uploaded from thousands of sources including all Asia official websites, Asia local websites, newspapers and journals. Bidding for Hiv Aids Medicine tenders in Asia is extremely lucrative for companies of all sizes. Asia tendering authorities release contracts for most of the Hiv Aids Medicine products and services procured by them. The most popular categories are -

  • Asia hiv tenders
  • Asia hiv aids medicine tenders
  • Asia hiv aids prevention tenders
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10 Live Notices for Asia Hiv Aids Medicine Tenders

Showing 1 to 10

Purchase Of Blank Products For 2025
country Kyrgyzstan
posting date24 Jan 2025
deadline07 Feb 2025
Supply of Medicine and Medical / Surgical equipments : Dried Recombinant Factor, VIII Fraction\n500IU vial\nDried Recombinant Factor VIII Fraction 500IU vial\nDried factor VIII Fraction BP (Dried Recombinant\nAntihaemophilic Fraction) 500IU vial\nOR\nRecombinant Coagulation Factor VIII Ph Eur.\n500IU vial\nOR\nRecombinant Antihemophilic Factor USP 500IU vial\nOR\nDried Recombinant Antihaemophilic Fraction IP\n500IU vial\nEach vial to contain 500IU of concentrated,\npurified and viruses inactivated 3rd or 4th\ngeneration recombinant dried factor VIII Fraction\nBP, Ph Eur, USP or IP.\nNote:\n1. The item should be stable at temperature 2oC –\n8oC.\n2. The product should have minimum 24 months\nshelf life at the time of delivery to MSD.\n3. Tenderer should submit detailed specifications\nof the product offered.\n4. The product should ensure, at least two steps\non virus inactivation as recommended by\nWHO/US.FDA\n5. The purification process should be specified by\nthe manufacturer.\n6. Each batch should be certified as free from HIV\nhepatitis and other viruses.\n7. Anti viral test methods used for screening for\nHIV and Hepatitis viruses should be declared by\nthe manufacturer. The test methods used should\nbe approved by WHO/US.FDA.\n8. Each vial to be supplied with suitable diluent.\n9. The product should be protected from light.\nPacking : 10 vials in a Pack etc .
country Sri Lanka
posting date16 Jan 2025
deadline25 Feb 2025
Supply of Medicine and Medical / Surgical equipments : Antitetanus Human Immunoglobulin 250IU\nAmpoule/Vial/Prefilled syringe\nAntitetanus Human Immunoglobulin 250IU\nAmpoule/Vial/Prefilled syringe\nEach ampoule/vial/prefilled syringe to contain\n250IU of Antitetanus Immunoglobulin obtained\nfrom Human Plasma containing specific anti\nbodies against Clostridium tetani suitable for\nintramuscular or intravenous injection.\nNote:\n1.This injection should be stable for 24 months\nwhen stored within a temperture range of 2'C-8'C.\nDo not freeze.\n2.The manufacturer should submit a certificate for\neach batch of the product that it has been tested\nfree of Hepatitis B,Hepatitis C and HIV infections.\n3.Each ampoule/vial/prefilled syringe should be\nlabelled accordingly. etc .
country Sri Lanka
posting date27 Dec 2024
deadline06 Feb 2025
Supply of Medicine and Medical / Surgical equipments : Dried Recombinant Factor VIII Fraction 200IU-\n350IU vial\nDried Recombinant Factor VIII Fraction 200IU-\n350IU vial\nDried factor VIII Fraction BP (Dried Recombinant\nAntihaemophilic Fraction) 200IU-350IU vial\nOR\nRecombinant Coagulation Factor VIII Ph Eur.\n200IU-350IU vial\nOR\nRecombinant Antihemophilic Factor USP 200IU-\n350IU vial\nOR\nDried Recombinant Antihaemophilic Fraction\nIP200IU-350IU vial\nEach vial to contain 200IU-350IU of concentrated,\npurified and viruses inactivated 3rd or 4th\ngeneration recombinant dried factor VIII Fraction\nBP, Ph Eur, USP or IP.\nNote:\n1. The item should be stable at temperature 2oC –\n8oC.\n2. The product should have minimum 24 months\nshelf life at the time of delivery to MSD.\n3. Tenderer should submit detailed specifications\nof the product offered.\n4. The product should ensure, at least two steps on\nvirus inactivation as recommended by\nWHO/US.FDA\n5. The purification process should be specified by\nthe manufacturer.\n6. Each batch should be certified as free from HIV\nhepatitis and other viruses.\n7. Anti viral test methods used for screening for\nHIV and Hepatitis viruses should be declared by\nthe manufacturer. The test methods used should\nbe approved by WHO/US.FDA.\n8. Each vial to be supplied with suitable diluent.\n9. The product should be protected from light. etc .
country Sri Lanka
posting date27 Dec 2024
deadline06 Feb 2025
Hainan Provincial Women And Children'S Medical Center-2024 Hainan Province Prevention Of Mother-To-Child Transmission Of Hiv, Syphilis And Hepatitis B Reagents And Drugs Procurement Project.
country China
posting date06 Jan 2025
deadline06 Jan 2026
Plan For Selecting Contractors For The Package: Providing Hall Rental Services And Related Services For The Course "Training On Guidelines For Developing Technical And Economic Norms For Medical Quarantine And Preventive Medicine Services" From November 7-8, 2024 In Hcm City Of The Global Fund For Hiv/Aids Technical Assistance Project For The Period 2024-2026 Sponsored By The Global Fund To Fight Aids, Tuberculosis And Malaria
country Vietnam
posting date25 Oct 2024
deadline25 Oct 2025
Itb-Procurement Of Drugs And Medicines, Medical Supplies, Dental & Laboratory Supplies And Hiv Testing Kits
country Philippines
posting date25 Jan 2025
deadline17 Feb 2025
Procurement Of Newborn Screening Test Kits
country Philippines
posting date23 Jan 2025
deadline31 Jan 2025
Procurement Of Drugs And Medical Supplies (Rhu) 2025
country Philippines
posting date15 Jan 2025
deadline04 Feb 2025
Tender Regarding Hiv Test Kit-1
country India
posting date23 Jan 2025
deadline06 Feb 2025

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