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MedTech Europe response to the consultation on Targeted Evaluation of In Vitro Diagnostic Regulation and Medical Devices Regulation
Posted on 25.03.2025
MedTech Europe recommendations to improve the EU Public Procurement Directive
Posted on 24.03.2025
MedTech Europe response to electronic Instructions For Use (eIFU) regulation revision
Posted on 20.03.2025
Joint discussion paper on the future governance of medical technologies in Europe
Posted on 19.03.2025
MedTech Europe report on Administrative Burden under IVDR and MDR
Posted on 18.03.2025
Digitalisation of Technical Documentation
Posted on 18.03.2025
Ensuring a smooth implementation and use of the EUDAMED Clinical Investigation and Performance Studies module
Posted on 18.03.2025
Submission of vigilance reports to Notified Bodies under EU MDR & IVDR
Posted on 17.03.2025
Joint statement on the crucial need to effectively fund health research and innovation in the upcoming European Framework Programme (FP10)
Posted on 13.03.2025
Exemption of Routine Blood Draws from Article 58.1(a) of the IVDR
Posted on 12.03.2025
Open letter: MedTech Europe calls for prioritising life sciences in EU Competitiveness strategy
Posted on 11.03.2025
Article 10a MDR and IVDR: Decision guide flowchart
Posted on 11.03.2025
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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 2,000,000 products and services on the market, medtech companies are improving patient outcomes and helping to make health systems more sustainable.