This webinar will cover all aspects of parvovirus filtration best practices: process development/optimization, pilot scale-up, and validation and explain the important connections between these activities. The rationale for the recommended best practices will be explained by discussing the underlying mechanisms that control filter performance.
In this webinar, you will learn about:
- how to measure filter performance and capacity
- how to optimize filter virus removal capability
- how to avoid potential pitfalls
Speaker
Paul Genest
Merck
Consulting Engineer
Paul Genest has a B.S. and M.S. in chemical engineering from the University of New Hampshire, USA. His graduate work/thesis involved converting a batch chromatography protein purification process into a continuous operation. He has since been an application engineer, focused on Mab protein purification (Koch Membrane Systems, Wyeth BioPharma, and Merck). He has many publications in the area of parvovirus filtration and 25 years of experience in the field working with these filters.
Pharma and biopharma manufacturing
- Downstream Processing
Duration:1h 15min
Language:English
Session 1:presented February 10, 2022
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