Join this webinar on the Environmental Monitoring System (EMS) for pharmaceutical cleanrooms and sterile manufacturing environments. Presented by Diego Bompadre, Sales Director at QSGroup, the session explores the latest regulatory expectations introduced by EU GMP Annex 1 (2022), the ISO 14644 cleanroom standards, and key data integrity principles. Participants will gain insights into cleanroom classification and monitoring, particle and viable contamination control, continuous environmental monitoring strategies, alarm and trend management, and the role of real-time monitoring technologies in ensuring compliance, product quality, and contamination prevention.
If you’ve already signed up for this webinar, enter your email below to access it.
– OR –
First time here? Complete the short form below and start watching right away.
Fill out the form below to register — you’ll get access to the webinar as soon as it’s available.
