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EU/EEA Market Access for “Swiss Legacy Devices” following entry into application of the MDR
Document - Posted on 03.08.2021
Open Letter: Call to action to ensure continued supply of medical technologies between the EU and Switzerland after 26 May 2021
Document - Posted on 10.05.2021
Impact of changes under the new EU IVD Regulation (EU) 2017/746 to international registrations
Document - Posted on 26.05.2020
Impact of changes under the new EU Medical Devices Regulation (EU) 2017/745 to international registrations
Document - Posted on 26.05.2020
Joint Statement on Global Harmonization of Ethical Business Principles in Medical Technology
Document - Posted on 02.05.2018
Global industry urges G20 trade ministers to fight against forced localization policies
Document - Posted on 01.08.2017
Access to Medical Technologies – Global developments
Document - Posted on 01.08.2017
International Regulatory Developments
Document - Posted on 01.08.2017
Developing Health Policies at the International Level
Document - Posted on 01.08.2017
European Unique Device Identification Database (EUDID) – 2014
Document - Posted on 01.08.2017
Joint Business call to a successful and inclusive conclusion of the EU-Japan EPA/FTA negotiations
Document - Posted on 16.06.2017
Joint Industry statement on EU-Japan FTA negotiations – 24 April 2014
Document - Posted on 29.04.2014
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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.