Navigating the EU Medical Device Regulation (MDR) hosted by U.S. Department of Commerce
The Medical Device Regulation (MDR) changed the European legal framework for medical devices and introduced new responsibilities for the European Medicines Agency (EMA) and for national authorities in the assessment of certain categories of products. The U.S. Commercial Service is inviting healthcare companies to join our webinar to hear directly from industry experts including Nina Brkuljan, Senior Commercial Specialist, U.S. Mission to the European Union, and Maria Duguine, PhD Chemistry, Consultant, RQMIS (EU/UK/US regulatory consulting firm) about the regulation and the current implementation strategy as well as learn the certification process, time commitment and resources needed to be successful.
Who Should Attend?
- Medical device producers including (stents, catheters)
- Medication producers that use certain applicators
- Certain cosmetics and food supplement producers