Standards
Access CDISC end-to-end Foundational and Therapeutic Area standards
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Working to amplify data's impact
CDISC creates clarity in clinical research by bringing together a global community of experts to develop and advance data standards of the highest quality. Together, we enable the accessibility, interoperability, and reusability of data for more meaningful and efficient research that has greater impact on global health.
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Global Regulatory Requirements
CDISC Standards are required for regulatory submissions to FDA (U.S.) and PMDA (Japan).
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