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EMA – Clinical Trials Information System designated as WHO primary registry

The Clinical Trials Information System (CTIS) has been designated as a primary registry by the World Health Organisation (WHO) within the International Clinical Trials Registry Platform (ICTRP). Becoming a primary registry means CTIS adheres to specific criteria for content, data quality and validity, accessibility, unique identification, technical capacity, and administration. This ensures comprehensive research information is accessible to healthcare decision-makers globally.

CTIS has already been a registered data provider for WHO since May 2023. Designation as a primary registry represents a significant milestone in facilitating data sharing and promoting transparency and trust in clinical research.

More information on the EMA Website.


OpenEdition vous propose de citer ce billet de la manière suivante :
vroby (19 mai 2025). EMA – Clinical Trials Information System designated as WHO primary registry. ELSIBI. Consulté le 16 mars 2026 à l’adresse https://doi.org/10.58079/13y62


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