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Healthcare-associated Infections
Document paper - Posted on 27.05.2013
Industry’s view on the future of in vitro diagnostic legislation in europe
Document paper - Posted on 08.05.2013
Pre-marketing authorization of new medical devices in the European Union and the United States
Document paper - Posted on 01.05.2013
EU Device regulation: Sickle cell patients fear delays
Document paper - Posted on 23.04.2013
What is MedTech Europe?
Document paper - Posted on 12.04.2013
Blood glucose monitors under WEEE
Document paper - Posted on 02.04.2013
Medical technology – contributing to Europe’s health, innovation and economy
Document paper - Posted on 10.03.2013
A need for separate legislation EDMA analysis of proposed regulation on in vitro diagnostic medical devices
Document paper - Posted on 01.03.2013
The MDD revision: What do patients & doctors think?
Document paper - Posted on 19.02.2013
MDD fact sheet: Delegated and implementing acts
Document paper - Posted on 30.01.2013
MDD fact sheet: Transition period
Document paper - Posted on 30.01.2013
MDD fact sheet: Funding
Document paper - Posted on 30.01.2013
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What we work on
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.
About us
MedTech Europe is the European trade association for the medical technology industry including diagnostics, medical devices and digital health.
About the industry
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.