European Commission publishes Version 22 of Q&A concerning Safety Features for Medicinal Products for Human Use
Medical Devices, Safety Features for Medicinal Products Elisabethann Wright Medical Devices, Safety Features for Medicinal Products Elisabethann Wright

European Commission publishes Version 22 of Q&A concerning Safety Features for Medicinal Products for Human Use

A consolidated version of the AI Act that includes revisions introduced in July 2026 has been published. Contrary to expectations in some corners, software as a medical device remain classified as high risk devices within the Act. There are a number of

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