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Procedural Guidance for Joint Scientific Consultations (JSC) on Medical Devices (MD) and In Vitro Diagnostic Medical Devices (IVD)

The Member State Coordination Group on Health Technology Assessment adopted this guidance pursuant to Article 3(7), point (f), of the Health Technology Assessment Regulation (Regulation (EU) 2021/2282).

This guidance defines detailed procedural steps and the timeframe for the conduct of JSC. It is the primary reference for Health Technology Developer and other stakeholders to comprehend key process steps and action points throughout the JSC procedure.

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). Procedural Guidance for Joint Scientific Consultations (JSC) on Medical Devices (MD) and In Vitro Diagnostic Medical Devices (IVD). ELSIBI. Consulté le 19 février 2026 à l’adresse https://doi.org/10.58079/141pc


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