致力于扩大数据的影响力
CDISC 通过汇聚全球专家群组来创建临床研究的清晰度，以便开发和开拓最高质量的数据标准。 我们共同促进数据的可及性、互操作性和可再用性以打造更有意义和更高效的研究，从而对全球健康产生更积极的影响力。
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Global Regulatory Requirements
CDISC Standards are now required for regulatory submissions to FDA (U.S.) and PMDA (Japan).
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