New medtech regulations

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

The Symbols Awareness Campaign goes live!

Symbols for compliance with the IVDR/MDR

MedTech Europe is driving the improvement of IMDRF Adverse Event Terminology

Progress in recognition of harmonised standards under MDR and IVDR

MedTech Europe’s reaction to the European Commission proposal to amend the In Vitro Diagnostics Medical Device and Medical Device Regulations

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