COCIR Statement on needed regulatory changes to the Medical Devices Regulation

With the adoption of Regulation (EU) 2017/745 (MDR), the regulatory framework for medical devices has changed significantly. The MDR is a welcome update for patient safety, transparency, and access to medical devices for European citizens.

COCIR calls for immediate action to avoid bottlenecks in MDR certification towards 2024 and to maintain access to the market for existing devices.

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