Browsing: regulatory affairs

Join our emergency briefing to learn about the U.S. Court of International Trade’s ruling on Trump Executive Orders and its implications for medical technology companies.

The European Commission has adopted an implementing regulation for joint scientific consultations on medical devices and in vitro diagnostic medical devices under the Health Technology Assessment (HTA) Regulation.

A summary of the 2025 Medical Device Recall Index Report, focusing on recall statistics, regulatory updates, and legal developments.