Europe Medical Devices Regulation (MDR) CE Marking Regulatory Process

EU CE Marking MDR process chart for medical devicesIn order to commercialize medical devices in the European Union, a CE Mark certificate is needed. This certification verifies that a device meets all regulatory requirements for medical devices, which will soon change under the new Medical Devices Regulation (MDR 2017/745). For a more detailed look at the European regulatory process for medical devices under the MDR, download the chart below.



Chart updated: 17/10/2018