GMP偏差调查中常见8大错误

2021-07-02 13:30  下载量:10

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By James Blackwell, Ph.D., The Windshire Group, LLC Deviation investigations are one of the most important quality activities in any GMP(good manufacturing practice) organization. They are also perennially near the top of the list of most frequently cited issues in observations, warning letters, and consent decrees from the U.S. Food and Drug Administration (FDA)and other regulatory authorities. (“There is a failure to thoroughly review [any unexplained discrepancy][the failure of a batch or any of its components to meet any of its specifications] whether or not the batch has been already distributed.”) 偏差调查是任何GMP组织中最重要的质量活动之一。在FDA和其他监管机构发布的缺陷、警告信和同意令中,它们也一直处于最常被引用的问题列表的首位。(“未能彻底审核[任何无法解释的差异][批次或其任何组分不符合质量,无论批次是否已经销售]。”)

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