Updated information pack for candidate EU reference laboratories published
In vitro diagnostic medical devices are tests intended for examination of human specimens for a medical purpose. In the EU, there is dedicated legislation that manufacturers must follow to produce and sell such devices. This legislation is Regulation (EU) 2017/746.
Read the news announcement published by EC Directorate-General for Health and Food Safety on 30 November 2022.
OpenEdition vous propose de citer ce billet de la manière suivante :
lsgilbert (24 janvier 2023). Updated information pack for candidate EU reference laboratories published. ELSIBI. Consulté le 16 mars 2026 à l’adresse https://doi.org/10.58079/o66h





