Europe – Study supporting the monitoring of the availability of medical devices on the EU market

Survey results of the 12th NB survey (MDR/IVDR) with data status 31 October 2024

Par
Pamela Cronin Bartolini
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Practical guidance for procedures related to Brexit for medicinal products for human and veterinary use within the framework of the centralised procedure

Commissioned by: The European Commission’s Directorate-General for Health and Food
Safety (DG SANTE) via the European Health and Digital Executive Agency (HaDEA)

• Aim: To support monitoring and analyzing the availability of medical devices on the EU market in the context of the implementation of medical devices and in vitro diagnostic medical devices Regulations from the perspectives of key stakeholders
• Duration: 2 December 2022 – 1 December 2025 (36 months)…

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