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This webinar will discuss the FDA requirements for design, validation and monitoring of pharmaceutical water systems. There are many different types of pharmaceutical waters and each must be fit for its intended use. Pharma water must be controlled microbially and for other impurities. Pharma water systems must be designed, validated and monitored to ensure that the water produced meets specifications around the clock. Learn common pitfalls with water system design and use and how to avoid them. Get your pharma water questions answered in this webinar.
Attend this webinar to learn in depth about pharmaceutical water, how to design systems for appropriate microbial control; to learn the minimum requirements for validation of pharmaceutical water systems. Also learn the different types of pharmaceutical water and their requirements and fitness for intended use and more.
Gwen Wise-Blackman, Ph.D., has 20 years of combined experience in Cell-Based Assays and Quality Systems. She has worked at DuPont Pharmaceuticals, Catalent Pharma Solutions (formerly Magellan Laboratories and Cardinal Health), and Salix Pharmaceuticals. She is currently Principal Consultant at Gwen Wise-Blackman Consulting. Her career focus has been in High-Throughput Screening, Cell-Based Assay Method Development and Validation, and Quality Assurance. Gwen has a Bachelor of Science degree in biology from M.I.T and a PhD in Pharmacology from UVa. She is a member of ASQ and AAPS
Speaker: Bruce Lee
Duration: 90 Minutes
Date: 19 September, 2025 (Friday)
Speaker: Jenny Douras
Duration: 60 Minutes
Date: 23 September, 2025 (Tuesday)
