MedTech Europe is calling on the European Commission and the MDCG to streamline the processes for evaluating vigilance data under the MDR and the MDIV in order to eliminate duplication in the review of vigilance reports.

Learn more

Linked news

The European Commission has released a new update to its study on the availability of medical devices in Europe

21 Jul 2026 Read more

Reusable Surgical Instruments and EU Regulation 2017/745

21 Jul 2026 Read more

Biological Evaluation of Medical Devices

21 Jul 2026 Read more
This site is registered on wpml.org as a development site. Switch to a production site key to remove this banner.