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International Regulatory Developments

Document paper - Posted on 01.08.2017

Developing Health Policies at the International Level

Document paper - Posted on 01.08.2017

European Unique Device Identification Database (EUDID) – 2014

Document paper - Posted on 01.08.2017

Joint Business call to a successful and inclusive conclusion of the EU-Japan EPA/FTA negotiations

Document paper - Posted on 16.06.2017

Joint Industry statement on EU-Japan FTA negotiations – 24 April 2014

Document paper - Posted on 29.04.2014

Eucomed Statement on NEJM article “Patient Access to Medical Devices – A Comparison of U.S. and European Review”

Document paper - Posted on 15.10.2013

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

Pre-marketing authorization of new medical devices in the European Union and the United States

Document paper - Posted on 01.05.2013

US PMA no more of a safeguard than EU CE mark yet

Document paper - Posted on 20.09.2012

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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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