Microbiology Testing: USP requirements for Sterile and Nonsterile Preparations

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  • เผยแพร่เมื่อ 27 พ.ค. 2024
  • This session identifies microbiology testing requirements for sterile and nonsterile preparations. USP microbiology general and informational chapters provide guidance related to sterility assurance, bacterial endotoxins and microbial quality requirements. Participants will learn how to apply USP guidance in pharmacy production, operations and design.
    Learning Objectives:
    At the conclusion of the program, the participants should be able to:
    (1) Explain testing requirements based on USP microbiology test general chapters
    (2) Interpret sterility test results and assess sterility test limitations
    (3) Identify areas of pharmacy operations that require environmental testing
    (4) Identify microbiological tests used in managing the production of nonsterile drug products

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