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Dynamic Purchasing System For Medical Technical Equipment.

Provision of health services, by THE INSTITUTION under its responsibility, with its own human, technical, administrative, locative, General Medicine, General Dentistry, Promotion and Prevention Programs, therapeutic support consultations, medical specialties, aids diagnostics and other services enabled according to the institution's service portfolio that is an integral part of the contract, prior authorization by the University and defined

Providing for for Medical Products for the ECOWAS Joint Assessment Procedure under the West Africa Medicines Regulatory Harmonization (WA-MRH)

San Gil Medical Services

Framework Agreement Cadry Condered National Program Hiv Aids

* Price Registration * Price Registration For Future Acquisition Of Medicines - Hiv/Aids 02. Protocol No. 23.146.702-5

Laboratory Diagnostic System And Reagents For The Execution Of The Confirmation Tests For Hiv 1 And 2, Hcv, Treponema With Immunoblot Technique

Dental Clinic'S Dental Clinic Equipment 2

Supply of Medicine and Medical / Surgical equipments : Elisa Test kit for detection of HIV P24 antigen\nand antibodies to HIV; HIV 2 and HIV vi sub\ntype „O‟ antigen\n1. Test kit should detect of HIV P24 antigen\nand antibodies to HIV-1 (groups M and O)\nand HIV-2 inhuman serum or plasma.\n2. Number of tests shall be performed =480\ntests per kit\n3. Sensitivity should be 100%\n4. Specificity should be more than 99%\n5. Residual shelf life at the time of delivery\nshould be minimum of 18 months\n6. Each test kit should include adequate\npositive and negative controls\n7. Shall give a color change once serum is\nadded to the reagents.\n8. Precautions must be taken to maintain the\ncold chain while transportation until it reaches\nthe blood bank, as these\nreagents are kept at 2-6C.\n9. Reagent brochure, labels and any other\ninformation provided should be in English\nlanguage.\n10. Reagent shall contain FDA certification\nand/or WHO certification/ EU Quality\ncertification /free sales certificate and\ncertificate of use in the country in country of\norigin/ end user evaluation certificate/ or free\nsales certificate in USA, UK, France, Germany,\nCanada, New Zealand or Australia with\nstandard quality certificates etc .

Supply of Medicine and Medical / Surgical equipments : HIV Ag/Ab Combo Reagent for Analyzer\nCMIA technology-based HIV Ag/Ab Combo\nassay for blood donor screening.\nThe reagent kit shall be compatible with\nAlinitys Analyzer. CMIA HIV Ag/Ab Combo 4th\ngeneration assay should use two step\nchemiluminescent microparticle enzyme\nimmunoassay (CMIA) used for the\nsimultaneous qualitative detection of human\nimmunodeficiency virus (HIV) p24 antigen and\nantibodies to HIV type 1 (HIV-1 group M and\ngroup O and/or type 2 (HIV-2) in human serum\nand plasma, including specimens collected\npostmortem (non-heart-beating) to be used on\nAlinity s system for blood donor screening\npurposes. Ready To Use cartridges for the\neasy of use and less manual intervention.\nEach cartridge should be able to perform 500\ntests.\nThe reagent kit must be FDA approved for\nblood donor screening of HIV and certificates\nshall be attached.\nThe reagent kit must be NMRA approved for\nblood donor screening of HIV for blood and\nplasma donors.\nAll certificates of NMRA mentioning donor\nscreening purpose must be submitted for HIV\nAg/Ab Combo reagents.\nThe CMIA technology-based HIV Ag/Ab Combo\nassay should include calibrator kits, control\nkits, release control kits and reaction vessels\nalong with the reagent kits. At the time of\ndelivery expiery time shall be minimum of 10\nmonths.\nPacking : 500 tests etc .