The European Union Medical Device Regulation/In-Vitro Diagnostics Regulation (EU MDR/ IVDR) should make for a healthier medical device landscape in the EU once implemented. But, as deadlines rapidly approach, how can companies prepare and set themselves up for ongoing success in the years to come? The online EU MDR & IVDR Virtual Summit, March 15 - 19, will help quality, regulatory and product development professionals understand the new EU medical device regulations and provide strategic ways for companies to be both successful and competitive in the European market once MDR and IVDR go into effect.
Sign up for free and get lifetime access to all of the presentations including one from ICS on Implementing and Maintaining Changes to SaMD Under MDR, and many more.