CDISC研究数据制表模型(SDTM)的发展与实现

F. Wood, Tom Guinter
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引用次数: 17

摘要

摘要临床数据交换标准联盟(CDISC)研究数据制表模型(SDTM)是向FDA提交数据制表以支持营销应用的标准。2004年7月,该标准成为电子通用技术文件(eCTD)指南中引用的FDA研究数据规范的一部分。本文将概述SDTM及其相关实施指南的发展和现状,这些指南通常被称为人体临床试验研究数据制表模型实施指南(SDTMIG)和非临床数据交换标准(SEND)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evolution and Implementation of the CDISC Study Data Tabulation Model (SDTM)
AbstractThe Clinical Data Interchange Standards Consortium (CDISC) Study Data Tabulation Model (SDTM) is a standard for submitting data tabulations to the FDA in support of marketing applications. In July 2004, this standard became part of the FDA Study Data Specification referenced in the electronic Common Technical Document (eCTD) Guidance. This article will provide an overview of evolution and status of the SDTM and the associated Implementation Guides, commonly referred to as the Study Data Tabulation Model Implementation Guide for Human Clinical Trials (SDTMIG) and the Standard for Exchange of Nonclinical Data (SEND).
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