In 2016, both PMDA (Japan) and the US FDA mandated the requirements to submit CDISC compliant data for regulatory reviews.

2016年开始，日本和美国的药物监管机构先后启动了递交符合CDISC标准的临床试验数据的强制性要求。

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As a new CDISC member, Hua will proactively work with its peers to contribute to the implementation of CDISC standards in the discovery and development of novel medications in China.

作为CDISC的新会员，华领医药将继续与同行群策群力，积极将CDISC标准实践于中国原创新药的研究和开发中。

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