Draft UK Medical Device Amending Regulations: Key Proposals and MHRA Call for Evidence

UK Government Considers New Regulations for AI-Powered Medical Devices in Healthcare

The MHRA is seeking evidence on the regulation of AI in healthcare to inform the recommendations of the National Commission into the Regulat

TÜV Association criticizes EU plans to reform Medical Device Regulation, citing patient safety risks

Why fewer unannounced audits endanger patient safety and why something must happen before action is taken, explains Mark Küller from TÜV.

Engineering Analysis of Health Wearables: How Medical Devices Balance Precision and Consumer Design

Experience the engineering behind today’s leading health wearables including Oura Ring, Dexcom G7, Omnipod, and Jabra Hearing Aids. Industri

A new phase for EU data governance, cross-border GDPR enforcement and the European Health Data Space

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Personal Reflection on Using Proprietary Medical Devices for Diabetes Management

I wrote last month about my diabetes diagnosis this year and my difficult choice to wear a proprietary device (called a CGM) on my arm 24/7

CELEX:32026R1451: Règlement délégué (UE) 2026/1451 de la Commission du 20 mars 2026 modifiant le règlement (UE) 2017/745 du Parlement européen et du Conseil en ce qui concerne la liste des dispositifs implantables et des dispositifs de classe III exemptés