The Future of EU Medical Technology Regulatory System

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

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

The Future of Europe’s Medical Technology Regulations

MedTech Europe Survey Report – Analysing the availability of Medical Devices in 2022 in connection to the Medical Device Regulation (MDR) implementation

MedTech Europe Survey Report – Analysing the availability of In vitro Diagnostic Medical Devices (IVDs) in May 2022 when the new EU IVD Regulation applies

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