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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.
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.