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The European Commission is preparing the revision of technical aspects of the Medical Device and the In Vitro Regulation to bring them in line with the AI Act, according to a meeting document seen by Euronews. Further certification rules under the Radio Equipment Directive, and toys and machinery rules will need to be adapted as well after the AI Act entered into force last August, the Commission told member states. The AI Act aims to regulate applications and tools according to the risks they pose to users and societies. The general-purpose AI rules will apply one year after entry into force …

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