In May 2017, a new Medical Device Regulation (MDR) was established across the European Union. Its objective is to validate the safety and efficacy of medical devices more thoroughly and proactively.
As a result, all Medical Device Manufacturers will need to show evidence of a consistent and proactive process to document their pre- and post-market clinical research activities for medical devices of all classes.
Download your free copy of the infographic and discover 5 specific steps you should take to better prepare for the new EU MDR, such as:
By the way, this infographic is best viewed on your mobile or desktop and not printed.