Guidance – MDCG endorsed documents and other guidance
This guidance is published to assist stakeholders in applying Regulation (EU) 2017/745 on medical devices (MDR) and Regulation (EU) 2017/746 (IVDR) on in vitro diagnostic medical devices. The guidance is endorsed by the Medical Device Coordination Group in accordance with Article 105 of the MDR and Article 99 of the IVDR.
Read the guidance published by Directorate-General for Health and Food Safety on 10 January 2025.
OpenEdition vous propose de citer ce billet de la manière suivante :
lsgilbert (26 février 2025). Guidance – MDCG endorsed documents and other guidance. ELSIBI. Consulté le 25 avril 2025 à l’adresse https://doi.org/10.58079/13ds0