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FAQ – RoHS 2 obligations for medical devices and IVDs
Document paper - Posted on 28.02.2014
Superbugs
Posted on 09.02.2014
Revision of Directive 98/79/ECON In Vitro Diagnostic Medical Devices
Document paper - Posted on 17.01.2014
European IVD Market Statistics Report 2013
Document paper - Posted on 01.01.2014
European In Vitro Diagnostics Industry – Facts and Figures
Document paper - Posted on 01.01.2014
The European medical technology industry in figures 2014
Document paper - Posted on 01.01.2014
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
Executive summary – slow burn: the need to transform the MedTech model in Europe
Document paper - Posted on 10.10.2013
Financial impact of the Revision of the EU Medical Devices Directives on European SMEs and industry
Document paper - Posted on 10.09.2013
Statement on nomenclatures used for regulatory purposes (such as registration) in the field of in vitro diagnostics
Document paper - Posted on 12.08.2013
Companion Diagnostics are enablers of Personalised Medicine
Infographic - Posted on 23.07.2013
In vitro diagnostics in healthcare pathways
Infographic - Posted on 23.07.2013
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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.