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  • WHO Workshop On GMP Outline

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    Waqas Ahmed Zaibi
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    WHO workshop on GMP, bioequivalence, prequalification aims To introduce the participants on latest concept of GMP. Introduce the Bioequivalency studies for Pharmaceuticals and highlight international requirement for bioequivalent studies. Introduce WHO prequalification program for medicines; structure of product documentation, principles. Of compilation of product documentation. Examples of deficiencies most frequently identified in submission for prequalification Feedback and way forward.

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    WHO Workshop on GMP Outline

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    WHO workshop on GMP, bioequivalence, prequalification aims To introduce the participants on latest concept of GMP. Introduce the Bioequivalency studies for Pharmaceuticals and highlight international requirement for bioequivalent studies. Introduce WHO prequalification program for medicines; structure of product documentation, principles. Of compilation of product documentation. Examples of deficiencies most frequently identified in submission for prequalification Feedback and way forward.

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    7 views2 pages

    WHO Workshop On GMP Outline

    Uploaded by

    Waqas Ahmed Zaibi
    WHO workshop on GMP, bioequivalence, prequalification aims To introduce the participants on latest concept of GMP. Introduce the Bioequivalency studies for Pharmaceuticals and highlight international requirement for bioequivalent studies. Introduce WHO prequalification program for medicines; structure of product documentation, principles. Of compilation of product documentation. Examples of deficiencies most frequently identified in submission for prequalification Feedback and way forward.

    Copyright:

    Attribution Non-Commercial (BY-NC)
    Download as DOCX, PDF, TXT or read online from Scribd
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    of 2

    WHO Workshop on GMP, Bioequivalence, Prequalification

    Objectives of the Workshop To introduce the participants on latest concept of GMP Promote International Nom and standards on Pharmaceutical manufacturing and quality Introduce the Bioequivalence studies for Pharmaceuticals and highlight international requirement for Bioequivalence studies To introduce WHO prequalification program for Medicines; structure of product documentation, principles of compilation of product documentation and other related requirements; examples of deficiencies most frequently identified in submission for Prequalification Feedback and way forward

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