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EU and US call for input on opportunities to promote greater regulatory compatibility in the medical technology sector

Document paper - Posted on 01.07.2013

Delineation between the Conformity Assessment requirements of the Medical Devices and the RoHS 2 Directives

Document paper - Posted on 06.06.2013

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

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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.

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About us

MedTech Europe is the European trade association for the medical technology industry including diagnostics, medical devices and digital health.

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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.

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