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The EU HTA Regulation: Webinar for health technology developers of medical devices and in vitro diagnostic medical devices

This webinar explained the process for joint clinical assessments and joint scientific consultations for high-risk medical devices and in vitro diagnostic medical devices, and the European Commission demonstrated 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 23 December 2025.

 


OpenEdition vous propose de citer ce billet de la manière suivante :
lsgilbert (11 février 2026). The EU HTA Regulation: Webinar for health technology developers of medical devices and in vitro diagnostic medical devices. ELSIBI. Consulté le 16 mars 2026 à l’adresse https://doi.org/10.58079/15nzd


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