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EU Q&A document on AI Act, medical-device rules interplay up for final approval

( June 11, 2025, 14:29 GMT | Official Statement) -- MLex Summary: The European Commission shared a question and answer, or Q&A, document meant to clarify the interplay between the EU AI Act and medical devices regulations, which the industry has criticized for not providing enough legal clarity on key tension points. The document includes a last-minute change indicating that additional guidance will be provided on the appropriate legal requirements for in-house medical devices using AI. The Q&A is now undergoing approval by written procedure, with the deadline set on June 14.Q&A document in attachment (in English)....

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