In collaboration with Biozeen.
Description: As sterile filtration remains a critical control step in biopharmaceutical manufacturing, regulatory bodies are raising the bar on what constitutes a robust and compliant filter validation program. This webinar will explore the evolving expectations from global regulators and auditors, and how organizations can adapt through advanced validation practices and dual filter strategies.
Designed for professionals in quality, regulatory, and process development functions, the session will address both foundational principles and cutting-edge developments in sterile filter validation.
Key Highlights:
- Importance of Filter Validation
- Common pitfalls and how to avoid audit observations
- Recent advancements in bacterial retention (BR) testing
- Troubleshooting filtration failures: root causes and corrective strategies
- The science and application of dual filter validation – when, why, and how
- Case insights and industry best practices
Speakers Dr. Christina Rosy J. & Mr. Aswath Kumar
Biozeen
Registration link will be available soon
