Free Webinar: Biocompatibility Testing: in vitro versus in vivo – Recent developments and acceptance throughout different regulatory authorities

ANJA FRIEDRICH

General Manager at Eurofins Medical Device Services France
Business Unit Manager Consulting France

DR. HELGE GEHRKE
Senior Scientific Director in vitro Toxicology and Alternative Methods

In this webinar, we will cover the latest regulatory updates in the context of the updated ISO 10993 standards, explore in vitro test methods and strategies, and compare acceptance by different global authorities including FDA and Notified Bodies. The theoretical background will be complemented by real case studies, challenges, and pitfalls to give practical insights who to navigate in this evolving landscape.

• Regulatory Affairs Professionals: Ensure compliance with changing biocompatibility requirements.
• Medical Device Manufacturers: Optimize testing strategies for faster approvals and cost efficiency.
• Quality & Risk Management Teams: Understand implications for product safety and risk assessments.
• R&D and Laboratory Specialists: Learn about innovative in vitro methods and their practical application.

Click here to register