Medical Device EU MDR 1-Day Seminar

4/11/2026   900-1600

This comprehensive seminar provides essential knowledge for navigating the EU Medical Device Regulation (MDR) 2017/745 requirements. Designed for medical device professionals, this program focuses on the practical application of regulatory tools and pathways for successful EU market access, using real-world examples and exercises to ensure effective compliance implementation.

Participants will gain a critical understanding of MDR requirements, transition strategies, and practical compliance approaches essential for maintaining EU market access in the post-MDD regulatory environment.

Through real-world examples and lessons learned, the seminar equips attendees with applicable tools to improve compliance and avoid common pitfalls.

Whether you're planning for certification, in the middle of the transition, or supporting MDR implementation, this course offers essential insights and actionable knowledge.

Target Audience:

• Regulatory Affairs professionals managing EU market access
• Quality Managers implementing MDR compliance systems
• Medical device manufacturers transitioning from MDD to MDR
• Business development professionals entering EU markets

Certification:

• Participants receive a Certificate of Completion documenting 8 hours of professional development in EU MDR compliance.