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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.

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About us

MedTech Europe is the European trade association for the medical technology industry including diagnostics, medical devices and digital health.

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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.

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