Source: Cytiva
Aseptic processing is critical to ensuring drug safety, and evolving global regulations are raising the bar, especially around filtration.
This article breaks down the growing importance of pre-use, post-sterilization integrity testing (PUPSIT) and updated Annex 1 guidelines, highlighting how manufacturers must balance contamination control with operational risk. It also explores how Cytiva supports compliance through advanced filtration systems, automation, and risk-based strategies that improve consistency and reduce human error.
Read the full article to understand how PUPSIT and Annex 1 requirements are shaping aseptic processing and how to implement them effectively while minimizing risk.
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