Environmental Monitoring and cleanroom qualification are critical parts of the EU’s guidance on good manufacturing practices. In the first part of our webinar series, our Annex 1 expert will provide a detailed analysis of the current regulatory requirements and what’s expected to change in the next revision regarding viable environmental and process monitoring, cleanroom qualification, and overall contamination control strategies.
Lucia Ceresa, PhD
Senior Technology and Market Development Manager
View the other webinars in the series:
- Keeping Up With Annex 1 Revisions: Impact of Major Changes (On Demand)
- Keeping Quality Control, Bioburden Testing, and New Technologies Current with Annex 1 (On Demand)
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