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MedTech Europe information leaflet on UDI and implant card availability
Document paper - Posted on 01.12.2021
Is the IVD Regulation Framework ready for Class D Devices?
Document paper - Posted on 21.10.2020
Ensuring a successful transition to the new IVD Regulation in light of COVID-19
Document paper - Posted on 09.07.2020
Industry Perspective on the Implementation Status of the MDR/IVDR
Document paper - Posted on 14.06.2019
MedTech Europe position on the proposed draft Standardisation Request for In-vitro Diagnostic Medical Devices (IVD) Regulation (2017/746/EU) and Medical Devices (MD) Regulation (2017/745/EU)
Document paper - Posted on 29.05.2019
The transition to a new regulatory framework for in vitro diagnostic medical devices in the European Union
Document paper - Posted on 30.05.2018
MDD fact sheet: Transition period
Document paper - Posted on 30.01.2013
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MedTech Europe plays an active role in ensuring that patients have access to safe, life-improving technologies. We are committed to making health systems more efficient and sustainable, helping to create a better future together.
MedTech Europe is the European trade association for the medical technology industry including diagnostics, medical devices and digital health.
The medical technology industry is a dynamic and innovative sector working to save and improve lives. With more than 500,000 products and services on the market, medtech companies are improving patient outcomes and helping to make health systems more sustainable.