6 Things You Need to Do to Prepare for the New EU Medical Devices Regulation
By Paul Brooks -
Published 15 June 2017
When the EU’s new Medical Devices Regulation (MDR) entered into force last month, it set in motion a three-year countdown to the new rules’ full application in 2020. For companies marketing devices in the EU that wish to continue to do so, there is a lot to do in that relatively short time, so it is critical to begin as soon as possible. Early preparation is key. Following are six things you should be doing to get ready.
Categories: Europe, EC, Medical Devices
Tags: Europe MDR, medical device regulation, new device regulations in Europe