European Medical Device Regulation 2017/745 (MDR) • The Future Starts Now

European Medical Device Regulation

The EU MDR will have sweeping effects on company audits, budgets and ROI assessments, and even CE mark certification. And, with 24 official EU languages to grapple with, MDR has presented myriad linguistic challenges, even to the most sophisticated medical device manufacturers.

It’s time to prepare—for May 2020 and beyond.