Getting Equipped for the Future with the New MAS-100 Sirius^® Microbial Air Sampler

WEBINAR

The environment for pharmaceutical production has changed massively over the last few years. A clear trend towards digitalization and automation is observable. New regulatory requirements have been set for GMP-compliant aseptic manufacturing to minimize contamination risks in cleanrooms.  In this webinar we will give an introduction to the portable new MAS-100 Sirius^® Microbial Air Sampler, which meets the new challenges. We will demonstrate how it supports regulatory compliance in a digital environment, minimizes handling errors and makes active air monitoring easier to perform.  Another key focus will be the validation process – highlighting what GAMP 5-based development is all about and how validation on customer side is supported.

What You’ll Learn:

• How the MAS-100 Sirius^® supports regulatory compliance in a digital environment
• Strategies to minimize handling errors and enhance active air monitoring
• Insights into the validation process for effective implementation

Who should attend?

This webinar will benefit professionals in the pharmaceutical industry, in particular:

• QA/QC managers and operational personnel in production
• IT experts for operational data handling