Webinar | Understanding PFAS: Risks, regulations, and fill & finish readiness
Thursday, October 8, 2026
Session 1: 10 a.m. CET | 2:30 p.m. IST | 5 p.m. HKT
Session 2: 8 a.m. PST | 11 a.m. EST | 5 p.m. CET
PFAS regulations are evolving rapidly across Europe, North America, and other global markets, creating uncertainty for biopharmaceutical manufacturers. While PFAS-containing materials play an important role in bioprocessing equipment, emerging restrictions may affect material selection, supply chains, validation strategies, and regulatory compliance.
In this webinar, Markus Maring and Dr. Lukas Raddatz will provide an overview of the current PFAS regulatory landscape, discuss the potential implications for biopharma manufacturing and sterile filtration, and share practical approaches for risk mitigation and future readiness. The session will also examine the challenges of replacing fluoropolymer-based materials, considerations for change control and product quality, and how next-generation filtration technologies like modified PES membranes can support performance, compliance, and sustainability goals.
What You Will Learn:
- Examine the evolving global PFAS regulatory landscape, including key restrictions, proposals, and industry discussions.
- Understand how PFAS regulations may impact biopharma manufacturing.
- Explore sterile filtration options and implementation strategies.