New medtech regulations

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

Updated! Medical Device Coordination Group vigilance Q&A document  

MedTech Europe‘s post-EPSCO statement on the necessary reforms of MDR/IVDR

Smooth transition to the mandatory use of EUDAMED

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

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

Medical Device Regulation & In Vitro Device Regulation – Article 10a implementation – EU Commission Q&A published

MedTech Europe reaction to the European Parliament’s Joint Motion for a Resolution on the urgent need to revise the Medical Devices Regulation

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

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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