Overview of language requirements for manufacturers of medical devices
Regulation (EU) 2017/745 on medical devices (MDR) contains different legal provisions that allow Member States to determine language requirements for manufacturers at national level for information accompanying the device. The following table gives an overview of the national provisions, in the case that Member States have made use of the possibility to determine language requirements for manufacturers.
Read the news announcement published by EC Directorate-General for Health and Food Safety on 20 March 2024.
OpenEdition vous propose de citer ce billet de la manière suivante :
lsgilbert (21 mai 2024). Overview of language requirements for manufacturers of medical devices. ELSIBI. Consulté le 16 janvier 2025 à l’adresse https://doi.org/10.58079/11ow4
