EU MDR: What’s new and what’s challenging?

The European Union's Medical Device Regulation (EU MDR), which came into effect in May 2021, has not only brought about significant changes to safety requirements but has also presented the medical device industry with a host of new challenges. Register to download this whitepaper to…

1. Understand the new safety requirements of the EU MDR and how they impact manufacturers.
2. Examine the hurtles that EU MDR poses for stakeholders in the medical device industry.
3. Learn 5 key challenges and solutions brought on by the implementation of EU MDR and the subsequent shift in the approach to clinical data collection and management for manufacturers.