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Join us for an exclusive webinar focused on the evolving landscape of pyrogen and endotoxin testing. With increasing emphasis on sustainability and regulatory modernization, this session will provide you with the insights and tools to confidently adopt non-animal, in vitro testing strategies.

In this webinar you will learn about:

• The role of sustainable endotoxin and pyrogen testing in reducing reliance on animal-based methods – and why it's critical for the future of biopharma QC
• Recent regulatory shifts driving adoption of recombinant and in vitro approaches, including updates from global authorities
• How to validate sustainable testing methods to support compliance and regulatory acceptance
• Best-fit testing strategies for when and where to apply each method throughout product development, validation, and routine quality control

Who should attend:

• QC lab managers/supervisors/directors
• QC lab analysts
• QA managers
• Process development scientists
• Method development scientists
• Sustainability managers
• Regulatory affairs managers

The webinar includes a Q&A session and will last approximately 30 minutes.

Unable to attend? Register now and receive an email notification as soon as the event is available for on-demand viewing.

We look forward to welcoming you.