Adapting to Annex 1: The Digitalization of Cleanroom and Aseptic Manufacturing Monitoring

Online webinar

The updated EU GMP Annex 1 brings stricter expectations for contamination control and continuous monitoring in cleanrooms and aseptic manufacturing. Meeting these standards is reimagining a future-ready, risk-resilient manufacturing environment.

This webinar explores practical ways to strengthen compliance, reduce manual errors, and boost operational efficiency.

What you will learn:

• Key changes in Annex 1 and how they impact your aseptic operations
• Why traditional monitoring methods may fall short under the new guidelines
• How digital Environmental Monitoring systems improve traceability and data integrity
• Best practices for automating cleanroom monitoring, alerts, and reporting
• Real-world use cases on how pharma companies are already benefiting from digital EM
• Steps to begin or accelerate your digital transformation journey

Join our expert-led session to learn how digitalizing EM systems can help you align better with Annex 1 requirements.