Commission designates new EU reference laboratories for high-risk in vitro diagnostic medical devices
Abstract
The European Commission has adopted an implementing act designating four EU reference laboratories in the field of in vitro diagnostic medical devices (IVDs). These laboratories will be involved in the conformity assessment of high-risk (class D) IVDs as well as in carrying out certain advisory tasks. Read the news published by DG Health and Food Safety on 18 December 2025.
Fields of Study & Subjects
Healthcare Regulation
Clinical Laboratory Practices and Quality Control
Biomedical Ethics and Regulation
Publication details
- Journal / source
- Hypotheses (OpenEdition)
- Publication date
- 11 February 2026
- Language
- EN