How the European Union Medical Device Regulation Affects Medical Device Innovation
The European Union Medical Device Regulation (MDR) is a set of rules and regulations that govern the safety and performance of medical devices in the European Union (EU). The MDR was implemented in May 2020 and is designed to ensure that medical devices are safe, effective, and of high quality. The MDR also seeks to promote innovation in the medical device industry by encouraging manufacturers to develop new and innovative products. The MDR has had a significant impact on medical device innovation in the EU. One of the key changes