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Transparency and Disclosure Interactions between Industry and Healthcare Professionals (HCP)
Document paper - Posted on 01.11.2012
Eucomed Statement on FDA Report “Unsafe and Ineffective Devices Approved in the EU that were Not Approved in the US”
Document paper - Posted on 15.10.2012
Community Care Sector Group at MedTech Europe
Document paper - Posted on 03.10.2012
Archive
Access to the Operating Room by Company Representatives
Document paper - Posted on 01.10.2012
Access to Ostomy Supplies and Innovation: Guiding Principles for European Payers
Document paper - Posted on 27.09.2012
Access to Ostomy Supplies and Innovation Guiding Principles for European Payers
Document paper - Posted on 20.09.2012
US PMA no more of a safeguard than EU CE mark yet
Document paper - Posted on 20.09.2012
Moving towards good practice in the reimbursement of CIED telemonitoring
Document paper - Posted on 29.08.2012
Financial times – Europe takes medtech lead
Document paper - Posted on 10.08.2012
EU regulatory framework for medical devices
Document paper - Posted on 23.07.2012
Perfecting the prosthetic leg
Document paper - Posted on 23.07.2012
Patient access to medical technology in the EU and US
Document paper - Posted on 23.07.2012
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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.