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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.
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.