The European Medical Device Regulation (MDR) is a new set of regulations that govern the production and distribution of medical devices in Europe. Compliance with the regulation is mandatory for medical device companies wanting to enter the European marketplace. Dr. Zwick, who has extensive experience in EU regulatory affairs will highlight some of the key changes that make up the MDR and their implications on the medical device industry. He will also discuss strategies to implement MDR successfully.
We invite you to join us in the final talk of the regulatory affairs webinar series to gain insights into essential topics from an expert on EU regulatory affairs.