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USP Microbiology 2020 - Essentials Of USP Microbiology Full Day Virtual Training
Topics/Call fo Papers
Microbiology plays a role throughout the manufacture of pharmaceutical products. Whether the final product is non-sterile or sterile, the bioburden exists within the raw materials,
Whether you are testing a starting material (component), an in-process sample, the Active Pharmaceutical Ingredient (API), final product (whether non-sterile or sterile), the environment to include controlled and classified areas,
Understanding the various General and General Information USP Chapters that apply to microbiology
Study the focus of the chapters to include those that primarily involve non-sterile and sterile applications and their interpretation
Speaker:
Barry A. Friedman, PhD, is a Consultant in the Biotechnology, Regulatory Compliance and Aseptic Processing Arena.
Whether you are testing a starting material (component), an in-process sample, the Active Pharmaceutical Ingredient (API), final product (whether non-sterile or sterile), the environment to include controlled and classified areas,
Understanding the various General and General Information USP Chapters that apply to microbiology
Study the focus of the chapters to include those that primarily involve non-sterile and sterile applications and their interpretation
Speaker:
Barry A. Friedman, PhD, is a Consultant in the Biotechnology, Regulatory Compliance and Aseptic Processing Arena.
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Last modified: 2020-10-22 00:51:56