EU restructures Website on Medical Devices
Recommendation
5/6 February 2026
A Tool to get Process Understanding
On the Road to 30,000 Members
Let us become the World's Leading GMP/GDP Compliance Community in 2026
A very helpful source of information on the regulation of medical devices is the website of the EU Commission. This has now been restructured. What does the new structure look like?
The new structure looks as follows: On the "Public Health" website, the topics listed are presented in non-alphabetical order in english. Here, you will find the medical devices, but also references to e.g. medicinal products. The medical devices are subsequently divided into six sections:
- Sector
- New regulations
- Topics of Interest
- Dialogue between interested parties
- Expert Panels
- EUDAMED
The sections are each linked to an overview, guidelines and highlights matching the section, latest updates, events and documents. However, there is some duplication in the highlights, latest updates, events and documents parts.
To find out more, please see the "Public Health" website.
Related GMP News
06.11.2025FDA Warning Letter Statistics on Medical Devices in the Past Fiscal Year 2025
06.11.2025FDA Breakthrough Device Program
06.11.2025US President Trump extends Transition Period for EtO Sterilisation
16.10.2025Overview of the FDA's new Quality Management System Regulation: effective from 2 February 2026
16.10.2025Survey of Notified Bodies on the Certification Procedure for Medical Devices
10.09.2025Artificial Intelligence in Medical Devices - the Perspective of Notified Bodies