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European IVD Market Statistics Report 2016
Document paper - Posted on 10.01.2018
Prioritising patient safety and public health across Europe post- Brexit
Document paper - Posted on 15.12.2017
Call for candidates to join the MedTech Europe Compliance Panel
Document paper - Posted on 01.12.2017
Global InVitro Diagnostic (GIVD) Classification – Version 2018
Document paper - Posted on 29.11.2017
Implementing the new IVD and Medical Devices Regulations – Transition Periods –
Document paper - Posted on 21.11.2017
Implementing the new IVD and Medical Devices Regulations – Early availability & capacity of notified bodies –
Document paper - Posted on 21.11.2017
Implementing the new IVD and Medical Devices Regulations – Resourcing and Governance –
Document paper - Posted on 21.11.2017
MedTech Week Magazine 2017
Document paper - Posted on 21.11.2017
Article 50 Negotiations between the EU and the UK (Brexit)
Document paper - Posted on 08.11.2017
European Commission launches action plan to decrease backlog of non-cited standards and to improve harmonisation process
Document paper - Posted on 31.10.2017
Educational Grant Request and Education Grant Agreement – Templates
Document paper - Posted on 19.10.2017
Leaflet for distributors on the new MedTech Europe Code
Document paper - Posted on 04.10.2017
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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.