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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.

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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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