Automating Success: Ensuring Annex-1 Compliance in Final Filtration

WEBINAR

In this webinar, you will learn:

• How Annex-1 requirements impact Final Filtration operations, focusing on PUPSIT implementation
• Why single-use assemblies can reduce patient and business risks
• How an automated system can optimize product recovery and your facility layout

Final sterilizing filtration is the critical last step in ensuring the sterility of medicinal products for human use. As single-use platforms gain traction in bioprocessing, a comprehensive approach is essential to guarantee the sterility of the entire system, including filters and components. With EU GMP Annex-1 mandating integrity tests on sterilized filter assemblies both before and after use, the complexity of manual operations increases, necessitating careful evaluation.

This is your opportunity to discover how our innovative solutions empower biomanufacturers to meet stringent regulatory requirements while enhancing their contamination control strategies.