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Support to medical education and interactions with Healthcare Professionals

Document paper - Posted on 04.07.2017

The use of the single registration number – Proposal for an IVD Regulation

Document paper - Posted on 20.04.2016

Requirement for a periodic safety update report – Proposal for an IVD Regulation

Document paper - Posted on 20.04.2016

Clinical evidence update – Proposal for an IVD regulation

Document paper - Posted on 20.04.2016

Requirements for point of care testing systems – Proposal for an IVD Regulation

Document paper - Posted on 20.04.2016

Concept of an IVD Kit

Document paper - Posted on 20.10.2015

Eucomed Position ahead of the trilogue on the Medical Devices Regulation

Document paper - Posted on 06.10.2015

Proposed regulation in IVD devices – Clinical evidence

Document paper - Posted on 28.09.2015

Comments on Council Approach on proposed regulation on In Vitro Diagnostic Medical Devices

Document paper - Posted on 25.08.2015

The revision of the EU Medical Devices Directives

Document paper - Posted on 27.07.2015

Revision of Directive 98/79/ECON In Vitro Diagnostic Medical Devices

Document paper - Posted on 17.01.2014

Financial impact of the Revision of the EU Medical Devices Directives on European SMEs and industry

Document paper - Posted on 10.09.2013

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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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