Rev. 1 – Q&A on practical aspects related to the implementation of Regulation (EU) 2023/607
This Q&A document is intended to facilitate the application of Regulation (EU) 2023/607 of the European Parliament and of the Council of 15 March 2023 amending Regulations (EU) 2017/745 (MDR) and (EU) 2017/746 (IVDR) as regards the transitional provisions for certain medical devices and in vitro diagnostic medical devices.
Read the news announcement published by EC Directorate-General for Health and Food Safety on 18 July 2023.
OpenEdition vous propose de citer ce billet de la manière suivante :
lsgilbert (5 septembre 2023). Rev. 1 – Q&A on practical aspects related to the implementation of Regulation (EU) 2023/607. ELSIBI. Consulté le 16 mars 2026 à l’adresse https://doi.org/10.58079/o6dm





