EMA To Get The Ball Rolling On Making CTIS Global

 
• By Vibha Sharma

The European Medicines Agency wants to further improve the visibility of data in the Clinical Trials Information System by establishing it as a World Health Organization primary registry.

Clinical Trial
CTIS Became A Data Provider For The WHO’s ICTRP Portal In 2023 • Source: Shutterstock

Keen to establish the EU Clinical Trials Information System (CTIS) as a trusted and accessible source of information on scientific research and knowledge, the European Medicines Agency is preparing to apply to the World Health Organization to make CTIS a WHO primary registry.

Primary registries in the WHO Registry Network need to meet specific criteria for content, quality and validity, accessibility, unique identification,...

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