Medical Device EU MDR Seminar – Regulation (EU) 2017/745

Medical Device EU MDR 1-Day Seminar

This comprehensive seminar provides essential knowledge for navigating the EU Medical Device Regulation (MDR) 2017/745 requirements.

Designed for medical device professionals, the seminar focuses on the practical application of regulatory tools, transition strategies and compliance pathways for maintaining successful EU market access in the post-MDD regulatory environment.

Through real-world examples, exercises and lessons learned, participants will gain practical tools to improve compliance and avoid common pitfalls.

Course Details

Duration: 1 day
Date: 04.11.2026
Hours: 09:00–16:00

What You Will Learn

• EU MDR 2017/745 requirements
• Practical regulatory tools and pathways for EU market access
• Transition strategies from MDD to MDR
• Practical approaches to MDR compliance
• Common compliance pitfalls and how to avoid them

Who Should Attend?

• 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 will receive a Certificate of Completion documenting eight hours of professional development in EU MDR compliance.

This seminar is part of the full Medical Device Quality and Regulation Course.