EU reference laboratories (EURLs)
The European Commission may designate EU reference laboratories (EURLs) for high-risk in vitro diagnostic medical devices according to Article 100 of Regulation (EU) 2017/746. The EURLs have two main categories of tasks: advisory ones and those related to conformity assessment, particularly of the highest risk, i.e., class D devices.
Read the news published by EC Directorate-General for Health and Food Safety on 7 November 2025.
OpenEdition vous propose de citer ce billet de la manière suivante :
lsgilbert (11 décembre 2025). EU reference laboratories (EURLs). ELSIBI. Consulté le 16 mars 2026 à l’adresse https://doi.org/10.58079/15bn8





