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Mattias Kyhlstedt, Michel Verhasselt, Michael Weisser

Webinar

EU HTA for Medical Devices and IVD’s

HTA (Health Technology Assessment) has long been used to evaluate certain medical devices and diagnostics. Now, a new EU HTA regulation is on the horizon, and it’s poised to bring major changes for the products it covers. This webinar is the first in a series exploring how the new EU HTA regulation might influence the MedTech and IVD industries. Even though many details of the regulation are still being finalized, we’ll share our perspective based on what we know so far and our experience in the field. In this session, we’ll cover:
- The history and current role of HTA in the medical device and diagnostics sector.
- Insights from EUnetHTA and what they mean for the future.
- Which products are eligible for EU HTA?
- An overview of the EU HTA process and how it works.
- Anticipated impacts in different countries – what to expect across Europe.
- A deep dive into how the EU HTA process might link to national decision-making, with a focus on:
 - Germany
 - France
- Recommended actions to help you prepare for these changes.

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