Staff working document on cost-savings for the proposal to reduce and simplify regulations on medical and diagnostic devices

In view of the challenges encountered in transitioning to the new requirements and to respond to the calls for urgent action from the European Parliament, the Council and a large number of stakeholders, the Commission brought forward the planned targeted evaluation of the Regulations to 2024. The targeted evaluation assessed the effectiveness, efficiency, relevance, coherence and EU added value of the Regulations. The evaluation also focused on the availability of devices in the EU on the de...