Medical Device Biocompatibility & Safety Summit 2025

Join global leaders in biocompatibility toxicology regulatory science and medical device innovation for a high-level two-day summit in the heart of Europe.

The Medical Device Biocompatibility & Safety Summit 2025 will deliver cutting-edge insights on ISO 10993 MDR FDA risk management testing and safety innovation — all while offering real-world guidance and networking with top stakeholders.

🎯 Why Attend?

• In-depth discussions on ISO 10993 MDR and FDA regulations
• Practical guidance on toxicological risk assessment & biological evaluation
• Expert-led sessions with case studies and live panels
• Strategic networking with RA/QA R&D CROs and manufacturers
• Explore the future of medical device safety compliance and innovation

👥 Who Should Attend:

• Regulatory Affairs & Quality Assurance Professionals
• R&D and Toxicology Scientists
• Biocompatibility & Clinical Evaluation Experts
• Medical Device Manufacturers
• CROs Testing Labs and Consultants
• Compliance Officers & Risk Managers

🎟️ Early Bird Offer:

Request early-bird registration access and group discounts by contacting:

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