Webinar - What do Regulators Check for when Auditing Cleaning and Cleaning Validation
David Waddington looks at the most common European and U.S. FDA regulatory findings related to basic cleaning issues including cross contamination and approaches to cleaning validation. He also highlights key changes in GMP guidance and discusses QP considerations such as the appropriate use of quality risk management and HBEL assessments.
NSF International, Health Sciences
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Country/Region:United Kingdom
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On CPHI since:2018
Other Content from NSF International, Health Sciences (1)
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News Brexit impact on UK pharma industry a moveable feast, industry experts tell CPHI Discover
The UK’s withdrawal from the European Union has meant the pharmaceutical industry has had to adapt to some monumental changes in terms of research, regulatory affairs, and trade. In this CPHI Webinar, three industry experts discussed what the future may hold for UK pharma in a post-Brexit world