In this free webinar, see how environmental monitoring in pharma supports contamination control, inspection readiness and a demonstrable state of control. Attendees will learn how to design a ...

Analysis: Monitoring-related enforcement actions grew nearly 200% between 2021 and 2025, according to a review of 3,286 FDA ...

Particle Measuring Systems have released a new on-demand E-Book focusing on environmental monitoring for the life sciences and pharmaceutical industry. This handbook is a timely addition to libraries ...

A new modification of the EU GMP Annex 1 regulatory standard for sterile drug products was announced in August 2022, substituting the most recent 2020 draft and the previous 2008 revision. The new ...

Biotech and pharmaceutical products must be manufactured in compliance with the current Good Manufacturing Practice (cGMP) regulations. Monitoring these areas meets the requirement for environmental ...

Before and after approval, all pharmaceutical products receive a mandatory stability trial. Post-approval stability trials continue to monitor quality throughout the product lifetime and storage ...

Discover how bioprocessing technology industrial applications expand as fermentation, membrane filtration, PAT, and ...

Effective environmental monitoring programs are defined not by how much data they collect, but by how quickly they trace data ...