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EU Regulation on HTA Striking the right balance for medical technology assessment
Document paper - Posted on 12.02.2024
Setting High Quality Standards in EU Regulation on HTA: Applying an Adaptive Approach to assess the value of medical technology innovation along the lifecycle
Document paper - Posted on 13.12.2023
EU HTA: MedTech Europe’s Recommendations for the Trilogue Negotiations
Document paper - Posted on 07.04.2021
Stakeholder involvement in HTA cooperation
Document paper - Posted on 20.09.2017
Position on future EU cooperation on Health Technology Assessment – March 2017
Document paper - Posted on 07.08.2017
Medical Device Industry Position on HTA – June 2017
Document paper - Posted on 25.07.2017
The value of industry involvement in HTA, November 2011
Document paper - Posted on 25.07.2017
HTA for IVDs in the Context of Market Access – June 2017
Document paper - Posted on 25.07.2017
Stakeholder involvement with the European HTA cooperation at strategic and operational levels, 11 May 2016
Document paper - Posted on 20.07.2017
Appropriate Stakeholder Consultation in EUnetHTA, 19 June 2013
Document paper - Posted on 20.07.2017
Stakeholder involvement in the EUnetHTA JA2 on HTA, 26 April 2012
Document paper - Posted on 20.07.2017
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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.