Factsheet for healthcare professionals and health institutions
In April 2017, the European Parliament and the Council adopted the Medical Devices Regulation (EU) 2017/745 and the In Vitro Diagnostic Medical Devices Regulation (EU) 2017/746. These two Regulations aim to create a robust, transparent, and sustainable regulatory framework that is recognised internationally, improves clinical safety and creates fair market access for manufacturers.
This factsheet is aimed at healthcare professionals and health institutions. For a general overview of the impact of the regulations please refer to the Medical Devices section on the European Commission website.
Read the news announcement published by EC Directorate-General for Health and Food Safety on 18 December 2024.
OpenEdition vous propose de citer ce billet de la manière suivante :
lsgilbert (12 janvier 2025). Factsheet for healthcare professionals and health institutions. ELSIBI. Consulté le 18 mars 2025 à l’adresse https://doi.org/10.58079/132ek