From Challenges to Opportunities: Navigating the EU MDR as a Medical Device Manufacturer
Do you sell your medical devices into the European market? If so, you’ll want to join leading experts from AtriCure, Axendia and Medidata as they discuss how the mandatory European Union Medical Device Regulation (EU MDR) governs the production and distribution of medical devices in Europe.
Join this webinar to learn about:
- The latest developments and timelines related to EU MDR compliance
- Strategies for addressing major challenges faced by the industry, including how AtriCure has addressed EU MDR requirements
- The necessary digital transformation to effectively meet EU MDR requirements and beyond