The Future of EU Medical Technology Regulatory System

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

Digitalisation of Technical Documentation

Ensuring a smooth implementation and use of the EUDAMED Clinical Investigation and Performance Studies module

Submission of vigilance reports to Notified Bodies under EU MDR & IVDR

Exemption of Routine Blood Draws from Article 58.1(a) of the IVDR

Urgent call for clarity on clinical strategy discussions

European medical technology industry calls for the EU to join the Medical Device Single Audit Program as a Full Member

MedTech Europe 2024 Regulatory Survey: key findings and insights

Smooth transition to the mandatory use of EUDAMED

Medical Technology Industry stands ready to support work on the future of the Medical Technology Frameworks

Open letter to Stella Kyriakides on the urgent need for action on the medical technology regulations

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

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