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Guidance for the selection of Medical Devices (MD) and In Vitro Diagnostic Medical Devices (IVD) for Joint Scientific Consultations (JSC)

The Member State Coordination Group on health technology assessment (HTA Coordination Group, adopted this guidance pursuant to Article 3 (7), in combination with Article 17(3) of the Health Technology Assessment Regulation (Regulation (EU) 2021/2282).

The present guidance document aims to make the eligibility criteria and the selection criteria for JSC explicit and to provide an interpretation of these criteria for medical devices and in vitro diagnostic medical devices.

Read the background document published by Directorate-General for Health and Food Safety on 15 April 2025.


OpenEdition vous propose de citer ce billet de la manière suivante :
lsgilbert (3 juin 2025). Guidance for the selection of Medical Devices (MD) and In Vitro Diagnostic Medical Devices (IVD) for Joint Scientific Consultations (JSC). ELSIBI. Consulté le 18 février 2026 à l’adresse https://doi.org/10.58079/141pb


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