MedTech Europe calls for simplification of EU digital legislation for medical devices
MedTech Europe has published a position paper proposing targeted reforms to ensure the coherent implementation of EU digital legislation affecting the medical technology sector. The paper responds to the European Commission’s regulatory simplification agenda and outlines recommendations to align horizontal digital laws with existing sector-specific frameworks, namely Regulation (EU) 2017/745, the Medical Devices Regulation (MDR), Regulation (EU) 2017/746, the In Vitro Diagnostic Medical Devices Regulation (IVDR), and Regulation (EU) 2025/327, the European Health Data Space (EHDS).