On-Demand Webinar: EU GMP Annex 1 Review, Insights, and Feedback
This on-demand webinar provides a summary of the new aspects of environmental monitoring per EU GMP Annex 1: 2022 in sterile manufacturing, and its potential implications for the Pharmaceutical industry.
The consultation document for the new Annex 1 revision provides insight into upcoming regulatory trends. In terms of environmental monitoring content, there is significant emphasis placed on manufacturers basing their decisions on scientifically sound and historical data, while applying a risk-based approach.
From a microbiology and particle contamination perspective, this document presents modern, relevant, and scientifically sound monitoring methods for the pharmaceutical manufacturing world. In addition, it covers a new and reasonable approach to trending and data analysis.
Watch this webinar to:
- Get Annex 1 reviews from various industry experts
- Find out what changes have been made and the impacts they will have on manufacturers
- Get insights and feedback from experts on the Annex 1 draft
- Learn what the updated Annex 1 might mean to your cleanroom manufacturing
- Answers to common questions
Complete the form at the right to access this webinar.
Are you prepared for the new EU GMP Annex 1? Particle Measuring Systems can help you with:
- Advisory Services: Risk Assessments, Quality Risk Management, and more
- Viable and non-viable particle counters
