Overview of language requirements for manufacturers of medical devices
The Commission and Member States have created MDR and IVDR tables. These tables aim to help manufacturers of medical devices and in vitro diagnostic medical devices, particularly small and medium-sized ones, understand the language requirements for the information and instructions that accompany a device in a specific country. The tables provide an overview of the language requirements for each Member State.
Read the general publication by EC Directorate-General for Health and Food Safety on 18 January 2024.
OpenEdition vous propose de citer ce billet de la manière suivante :
lsgilbert (13 février 2024). Overview of language requirements for manufacturers of medical devices. ELSIBI. Consulté le 19 janvier 2025 à l’adresse https://doi.org/10.58079/vts5
