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Reflection Paper: Lessons Learnt from the COVID-19 Pandemic and Recommendations on Purchasing Models
Document - Posted on 02.02.2021
Recovery/Resilience Agenda: Integration of digital health in the EU healthcare systems
Document - Posted on 18.01.2021
Is the IVD Regulation Framework ready for Class D Devices?
Document - Posted on 21.10.2020
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
Reflection paper on Sustainable and Effective Stockpiling for Emergency Preparedness
Document - Posted on 16.09.2020
Ensuring a successful transition to the new IVD Regulation in light of COVID-19
Document - Posted on 09.07.2020
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
COVID-19 Implications for Clinical Investigations Needed for Medical Device Recertification
Document - Posted on 27.05.2020
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
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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.