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Proposal for a REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL amending Regulations (EU) 2017/745 and (EU) 2017/746 as regards simplifying and reducing the burden of the rules on medical devices and in vitro diagnostic medical devices, and amending Regulation (EU) 2022/123 as regards the support of the European Medicines Agency for the expert panels on medical devices and Regulation (EU) 2024/1689 as regards the list of Union harmonisation legislation referred to in its Annex I

Dokument 1201356 · 16. dec. 2025 · Modtaget 17. dec. 2025 · Sidst opdateret 18. dec. 2025 · Forslag til forordning · Offentligt

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1_DA_annexe_proposition_part1_v2.pdf
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1_DA_ACT_part1_v2.pdf
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