Information note on joint assessments under the new regulations on Medical Devices
EC 13 Novembre 2017
Regulation (EU) 2017/745 on medical devices (the MDR) and Regulation (EU) 2017/746 on in vitro diagnostic medical devices (the IVDR)were published on 5 May 2017 and entered into force on 25 May 2017.
As of 26 November 2017, under one or both Regulations, any conformity assessment body already designated under the Medical Devices Directives or any new conformity assessment body may submit an application for designation [...]






























