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The revision of the EU Medical Devices Directives

Document paper - Posted on 27.07.2015

Revision of Directive 98/79/ECON In Vitro Diagnostic Medical Devices

Document paper - Posted on 17.01.2014

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

Industry’s view on the future of in vitro diagnostic legislation in europe

Document paper - Posted on 08.05.2013

EU Device regulation: Sickle cell patients fear delays

Document paper - Posted on 23.04.2013

MDD fact sheet: Transition period

Document paper - Posted on 30.01.2013

Working for you – Regulations and industrial policies

Document paper - Posted on 11.04.2011

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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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