制药公司如何为监管机构处理性健康研究的数据?

Annual review of sex research Pub Date : 2005-01-01
Maria Dilleen, Scott Haughie
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引用次数: 0

摘要

我们简要概述了统计输入对制药工业临床试验研究以及与监管机构互动的重要性,特别着重于统计学家在将新药推向市场所需的临床试验第2和第3阶段性健康项目中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
How do pharmaceutical companies approach data from sexual health studies for regulatory agencies?

We briefly outline the importance of statistical input into clinical trial research in the pharmaceutical industry and in interactions with regulatory agencies, with particular concentration on the role of the statistician in projects on sexual health during Phases 2 and 3 of clinical trials required in bringing new drugs to the market.

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