EU Reference Laboratories (EURLs) are scientific laboratories designated by the EU Commission to verify the performance and compliance of high-risk (Class D) IVDs. In particular, by performing batch testing and providing expert scientific advice to regulatory bodies and notified bodies regarding their conformity assessment process. They essentially act as quality control for the most critical IVDs on the market.
As of 1 January 2025, the first six EURLs are operational, covering the following areas:
For more information, please visit this page on the European Commission website.