EU news..

The implementation of the 2017 EU Medical Device Regulation (MDR17) has been a difficult process for a variety of reasons. The problems have been acknowledged by the European Commission who have recently launched a public consultation as part of what it calls a 'targeted revision' of the regulations. The stated aim is "to streamline and future-proof the regulatory framework by reducing the administrative burden and enhancing predictability and cost-efficiency, while preserving a high level of public health and patient safety".

This page was last updated: 22 Sept 2025