• Information for Suppliers

    Quality Assurance Policy for Diagnostics Products amended in February 2014

    • QA Policy for Diagnostics Products QA Policy for Diagnostic Products (“QA policy”) as issued on 14 December 2010 amended in February 2014
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    • Quality Assurance Policy for DiagnosticsThe Expert Review Panel mechanism Presentation
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    • Invitation to manufacturers of Rapd Diagnostic Tests (RDTs) for HCV, Syphilis (treponemal tests) and dual detection of HIV and HCV or HIV and HBV infections to submit an Expression of Interest (EoI) for product evaluation by an Expert Review Panel for Diagnostics (ERPD) 
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      Submission deadline: 28th September 2015
    • Expert Review Panel for Diagnostics (ERPD) - Lessons learned from the Pilot round
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    • ERPD Product questionnaire  
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    • Expert Review Panel for Diagnostics-Terms of Reference
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    Click here for details.

    Quality Assurance Policy for Pharmaceutical Products

    Quality Control Drug Testing Laboratory for Global Fund quality monitoring activities

    Questionnaire on the technical proficiency of QC Drug Testing Laboratories
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    We are using this information to provide PRs with a List of QC

    Laboratories meeting Global Fund requirements, along with a list of WHO-prequalified laboratories who have responded to the questionnaire.