The Future of EU Medical Technology Regulatory System

Sampling under In Vitro Diagnostics Regulation: MedTech Europe proposal for a more risk-based approach

Just published: amending electronic Instructions for Use regulation for medical devices

European Medical Device Nomenclature required for Medical Device Regulation and In Vitro Diagnostic Regulation submissions

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

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

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