This document provides a strategic and in-depth overview of the impact of Medical Device Regulation (MDR) on our industry sectors and is addressed to all parties involved in the concrete implementation the MDR. It outlines COCIR’s views articulated in four key areas.
The implementation process is now at a critical phase, with secondary legislation under development. As one of the lead industry stakeholders, COCIR has developed a detailed analysis of the impact on businesses and is constantly developing regulatory intelligence. COCIR to be highly supportive of the Member States and the European Commission and is ready to support them in the successful implementation.
Download the position paper here.