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FDA Requirements 2021 - The Microbiology of Water in a GMP Environment; USP, EP, JP and FDA Requirements for Potable Water, Purified Water, Water for Injection and Steam Webinar



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Knowledge of the microbiology of water in a GMP environment is critical to the health of any water system being used to produce a pharmaceutical or biotechnology product. Even companies manufacturing tablets need to be aware of the quality of the water that may be contacting their process or product.
The objective of this live and interactive WCS webinar is to assist those involved in the development of a process or the manufacturing of a product to explore water, as a raw material (component) in a GMP environment,
How to set up a water sampling system and its test frequency.
Determining the “Health” of a water system based upon test results.
What are the differences between USP, EP and JP water requirements
Barry A. Friedman, Ph.D., is a Senior Consultant in the Biotechnology, Regulatory Compliance, Microbiology and Aseptic Processing arena.

Last modified: 2021-03-23 23:25:18