New medtech regulations

Leaflet: Towards a revised EU regulatory framework for medical devices

Towards a revised EU Regulatory Framework for medical devices

MedTech Europe responds to the European Commission’s targeted evaluation of Medical Devices Regulation and In Vitro Diagnostic Medical Devices Regulation

MedTech Europe and industry partners call for stronger future governance of medical technologies

Ensuring an efficient implementation and use of the EUDAMED Clinical Investigation and Performance Studies module

The Medical Device Coordination Group In Vitro Diagnostic Medical Devices Classification Guidance revises SARS-CoV-2

MedTech Europe response to the consultation on Targeted Evaluation of In Vitro Diagnostic Regulation and Medical Devices Regulation

MedTech Europe response to the consultation on Targeted Evaluation of In Vitro Diagnostic Regulation and Medical Devices Regulation

MedTech Europe response to electronic Instructions For Use (eIFU) regulation revision

The Future of EU Medical Technology Regulatory System

Joint discussion paper on the future governance of medical technologies in Europe

MedTech Europe report on Administrative Burden under In Vitro Diagnostics Regulation and Medical Devices Regulation

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