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3 products newly prequalified PDF

Guideline/guidance

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3 products newly prequalified PDF

Guideline/guidance

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30th Edition of Prequalified Quality Control Laboratories List PDF

Guideline/guidance

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34th Edition of Prequalified Quality Control Laboratories List

Guideline/guidance

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35th Edition of Prequalified Quality Control Laboratories List PDF

Guideline/guidance

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36th Edition of Prequalified Quality Control Laboratories List PDF

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3rd Biotherapeutic Product (BTP) and Similar Biotherapeutic Product (SBP) assessment training (Virtual) - 14 June 2024 - Agenda PDF

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3rd Biotherapeutic Product (BTP) and Similar Biotherapeutic Product (SBP) assessment training (Virtual) - 14 June 2024 - AGENDA PDF

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3rd Invitation to quality control laboratories (QCLs) to submit an expression of interest for prequalification to the WHO Prequalification Team: medicines (1 June 2011) PDF

Guideline/guidance

Recently Updated Documents

Cold Chain Information Systems (CCIS) Guidance

PQDx_173 Abridged PQ assessment

Prequalification assessment fees for IVDs (PQDx_299)

Overview of WHO’s prequalification procedure for in vitro diagnostics (PQDx_007)

Instructions for completion of the Expression of interest form for WHO’s performance evaluation of in vitro diagnostics (PQDx_461)

WHO Technical Report Series Location

WHO Technical Report Series documents relating to development, production, distribution, inspection and quality control of medicines can be found in the guidelines section of the WHO web pages dealing with quality assurance of medicines. The guidelines most relevant to WHO medicines prequalification are listed and accessible on the WHO Technical Report Series page.