The extended transition periods concern devices that require involvement of a notified body for conformity assessment under Regulation (EU) 2017/746 and that have a certificate and/or a declaration of conformity...
Common specifications are detailed practical rules setting out how particular types of devices should comply with certain requirements of Regulation (EU) 2017/746...
The expert panel is one of the independent scientific bodies established by the Regulations on medical devices and Commission Implementing Decision 2019/1396...
There are a number of guidance documents endorsed by the Medical Device Coordination Group to assist stakeholders with the implementation of the medical device regulations...
