COCIR welcomes the publication of the legislative proposal for a targeted revision of the Medical Devices Regulation (MDR). We thank the European Commission for its efforts to address the challenges observed with the implementation of the current framework over the past eight years.
This revision is a cornerstone for the European Commission to deliver on its political guidelines to increase the competitiveness and attractiveness of Europe. COCIR fully supports the overall simplification objective while maintaining a high level of patient safety.