Who should write AI rules for medical devices? Commission ‘blank cheque’ divides lawmakers

EU PERSPECTIVES - The revision of the EU's medical device rules is exposing a wider disagreement over how AI should be regulated in healthcare. While industry and some lawmakers argue for less duplication between the Medical Device Regulation and the AI Act, others warn against giving the Commission too much discretion over future requirements.  Read more

"Not enough": Tiemo Wölken on the EU's AI rules for medical devices / Photo: European Parliament