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Clinical Evidence Requirements for CE certification under the in vitro Diagnostic Regulation in the European Union
Document - Posted on 28.05.2020
COVID-19 Implications for Clinical Investigations Needed for Medical Device Recertification
Document - Posted on 27.05.2020
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
MedTech Europe’s Facts and Figures 2020
Document - Posted on 20.05.2020
Responding to the COVID-19 Pandemic: the Diagnostic Industry Angle
Document - Posted on 18.05.2020
Protective Equipment in the context of COVID-19
Document - Posted on 11.05.2020
Access to medical technologies and services during the COVID-19 pandemic – Diabetes
Document - Posted on 23.04.2020
The Medical Technology Community Stands with Patients – Access to Medical Technologies and Services During the COVID-19 Pandemic
Document - Posted on 16.04.2020
European Industry trade and supply chain needs to respond to Covid-19
Document - Posted on 14.04.2020
What Types of Diagnostic Tests Exist to Detect COVID-19?
Document - Posted on 14.04.2020
Community Care – Best Practices
Document - Posted on 08.04.2020
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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.