New medtech regulations

COCIR and MedTech Europe support focus on the medical technologies regulatory system for Health Commissioner

Support from the medical technology industry for the ongoing EU-Switzerland negotiations

European Commission survey for healthcare professionals: Electronic Instructions for Use for medical devices

Manufacturer’s Declaration in relation to Regulation (EU) 2024/1860

New Substance of Human Origin Regulation

Letʼs Go Digital: Instructions For Use – Factsheet for healthcare professionals

Medical Devices Regulation (MDR): New symbols for medical devices – Factsheet for healthcare professionals

Adopted amendments to IVDR/MDR: more measures still needed to ensure that existing and new medical technologies reach patients and health systems

MedTech Europe welcomes the adoption of the Substances of Human Origin Regulation

European Parliament votes to amend IVDR and MDR

Call for feedback on electronic instructions for use for near-patient testing devices

European Parliament votes to amend IVDR and MDR

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