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CDISC Roadmap

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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.

Global Regulatory Requirements

CDISC Standards are required for regulatory submissions to FDA (U.S.) and PMDA (Japan).

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Use Cases for Clear Data

Learn how organizations have applied CDISC Standards to bring clarity to data.

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