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Coronavirus emergency vs. GDPR security standards (COVID-19 Q&A)
Document - Posted on 24.09.2020
MedTech Europe Code Guidance on COVID-19 Emergency Support (27 March 2020)
Document - Posted on 21.09.2020
The Value-Based Procurement Journey in Europe
Document - Posted on 17.09.2020
Reflection paper on Sustainable and Effective Stockpiling for Emergency Preparedness
Document - Posted on 16.09.2020
MedTech Europe Response to the Inception Impact Assessment on the Proposal for a Legal Act with Requirements for Artificial Intelligence
Document - Posted on 10.09.2020
A Vision for Digitally Enabled Diabetes Care in Europe
Document - Posted on 09.09.2020
Ensuring a successful transition to the new IVD Regulation in light of COVID-19
Document - Posted on 09.07.2020
Joint MedTech Europe/ EFPIA White Paper on Companion Diagnostics under the IVDR
Document - Posted on 17.06.2020
Event report – 1st European Value-Based Procurement Conference: a new paradigm in health care
Document - Posted on 11.06.2020
The need for ‘virtual audits’ under the Medical Device and In Vitro Diagnostic Regulations in the context of a pandemic, such as COVID-19
Document - Posted on 10.06.2020
MedTech Europe’s Guidance on Basic UDI-DI Assignment
Document - Posted on 02.06.2020
Clinical Evidence Requirements for CE certification under the in vitro Diagnostic Regulation in the European Union
Document - Posted on 28.05.2020
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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.
MedTech Europe is the European trade association for the medical technology industry including diagnostics, medical devices and digital health.
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.