INT/1116 Follow-up from the Commission

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Medical devices and in vitro diagnostics/Simplification
(mandatory opinion)
(COM(2025) 1023 final
EESC- 2025/04298 ‒ INT/1116
605th Plenary Session – April 2026
Rapporteur: Danko RELIĆ (HR-III) 
DG SANTE – Commissioner VÁRHELYI

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  • Follow-up from the Commission INT/1116

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Related content

Proposal for a Regulation - Targeted revision of the EU rules for medical devices and in vitro diagnostics

Usvojeno on 29/04/2026 - Bureau decision date: 02/12/2025
Referentni dokument
INT/1116-EESC-2025-04298-00-00-AC-TRA
Referral
COM(2025) 1023 final 2025/0404 COD
COM(2025) 1023 final 2025/0404 COD
Rapporteur
Danko RELIĆ
Civil Society Organisations - GR III
Croatia
Plenary session number
605
-

This initiative aims to simplify EU legislation on medical devices and diagnostics to enhance competitiveness, foster innovation and ensure proportionate, cost-effective safety requirements while maintaining high levels of patient protection and public health.

  • Record of proceedings INT/1116
Download — Mišljenje EGSO-a: Proposal for a Regulation - Targeted revision of the EU rules for medical devices and in vitro diagnostics
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