Updates on the applications for designation as a notified body under the MDR and the IVDR

The European Commission updated the available information on the applications for designation as a notified body under Regulations (EU) 2017/745 on medical devices (MDR) and 2017/746 on in vitro diagnostic medical devices (IVDR) as an Overview at each stage of the process. For more, see the Commission’s webpage on Notified Bodies.