Why airborne particulates matter in sterile manufacturing
How cleanroom classification differs from routine monitoring
How ISO 14644-1, EU GMP Annex 1 and FDA cGMP connect
Why 21 CFR Part 11 matters for electronic records and signatures
Making sense of Cleanroom Regulations
About the Event
Airborne particle monitoring is a core part of contamination control in sterile manufacturing. Cleanroom teams need to understand how regulations apply to classification, routine monitoring, electronic records and internal risk assessment.
Join Making Sense of Cleanroom Regulations, led by Nicole Aguilar, MSc, Global Product Manager, for a practical review of cleanroom requirements in pharma and biopharma environments.
In this webinar, you’ll learn:
This session is designed for quality, manufacturing, microbiology, environmental monitoring and contamination control teams that need to connect regulatory expectations with daily cleanroom decisions.
2026-GBL-EN-109975-v1