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The EU HTA Regulation: Webinar for health technology developers of medical devices and in vitro diagnostic medical devices (12 December 2025)

In this webinar, Chairs and Co-chairs of the Member State Coordination Group on Health Technology Assessment and its subgroups will explain the process for joint clinical assessments and joint scientific consultations for high-risk medical devices and in vitro diagnostic medical devices.

The European Commission will also demonstrate the HTA IT Platform which is used for secure exchange of information with health technology developers.

Read the news published by EC Directorate-General for Health and Food Safety on 21 October 2025.


OpenEdition vous propose de citer ce billet de la manière suivante :
lsgilbert (25 novembre 2025). The EU HTA Regulation: Webinar for health technology developers of medical devices and in vitro diagnostic medical devices (12 December 2025). ELSIBI. Consulté le 13 janvier 2026 à l’adresse https://doi.org/10.58079/157h4


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