Webinars: Medical

MDR Effects on Medical Device Processing


The new Medical Devices Regulation (2017/745/EU) (MDR) brings EU legislation into line with technical advances, chang­es in medical science, and progress in law making. There are many updates that effect reusable medical device manufacturers. This presentation will outline all of the testing and documentation that needs to occur prior to the MDR deadline.

Speakers:

Emily Mitzel M.S, B.S, Technical Consulting Manager, Sr. Scientist, Nelson Labs