USP Microbiology 2020 - Essentials Of USP Microbiology Full Day Virtual Training

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, throughout the process and/or within the product's environment
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.