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Implementing the New MD and IVD Regulations: Industry Calls for Solutions to Ensure Continuity of Care to Patients
Document paper - Posted on 26.07.2018
Notified Bodies: Key Pillar of the Medical Technology Regulatory System
Infographic - Posted on 26.07.2018
The transition to a new regulatory framework for medical devices in the European Union
Document paper - Posted on 30.05.2018
The transition to a new regulatory framework for in vitro diagnostic medical devices in the European Union
Document paper - Posted on 30.05.2018
Implementing the new IVD and Medical Devices Regulations – Transition Periods –
Document paper - Posted on 21.11.2017
Implementing the new IVD and Medical Devices Regulations – Early availability & capacity of notified bodies –
Document paper - Posted on 21.11.2017
Implementing the new IVD and Medical Devices Regulations – Resourcing and Governance –
Document paper - Posted on 21.11.2017
Medical Devices Regulation – Flowchart
Document paper - Posted on 15.09.2017
IVD Regulation – Flowchart
Document paper - Posted on 15.09.2017
MD and IVD training overview (non-profit) – 2017
Document paper - Posted on 23.08.2017
Links to relevant articles (15 June – 15 July 2017)
Document paper - Posted on 17.07.2017
Support to medical education and interactions with Healthcare Organisations
Document paper - Posted on 04.07.2017
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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.