Navigating through the Jungle of Biocompatibility and Beyond

Join us for a focused full‑day on‑site workshop dedicated to the latest regulatory updates, global requirements, and practical case discussions in biocompatibility, biological evaluation, and packaging validation.

Register now! 

📅 Date: 23.04.2026

🕘 Time: 08:30 – 16:00

📍 Location: Van der Valk Hotel Utrecht, Winthontlaan 4-6, 3526 KV Utrecht, Netherlands

💬 Language: English

💶 Participation Fee: €250

Why Attend?

This workshop is ideal for professionals in R&D, QA/RA, Regulatory Affairs, Packaging Engineering, and Product Development, offering:

• A comprehensive overview of the latest updates in ISO 10993‑1:2025 and their implications for biological evaluation
• Practical guidance on implementing risk‑based biocompatibility strategies supported by real case examples
• Insights into diverging FDA and EU biocompatibility expectations and how to build a cohesive global strategy
• An update on recent ISO and USP developments influencing biological safety assessments
• Clear methodologies for managing change assessments and maintaining compliance in a shifting regulatory environment
• A step‑by‑step walk‑through of ISO 11607‑based packaging validation, including shelf‑life assessment, transport simulation, and sterile barrier integrity testing
• Direct interaction with Eurofins scientific experts and opportunities for in‑depth discussion

Want to learn more?

More details and the full agenda are in the Flyer below.

For any information you can contact us at: medical-device@mds.eurofinseu.com