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首页> 外文期刊>Procedia Manufacturing >Manufacturing Pharmaceutical Medicines in a Regulated Environment - An Auditor’s Perspective
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Manufacturing Pharmaceutical Medicines in a Regulated Environment - An Auditor’s Perspective

机译:制造药物在监管环境中 - 审计员的观点

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摘要

The impact of the appropriate and inappropriately applied statistical metrics to verify the State of Control of pharmaceutical manufacturing has been reviewed from an auditor’s perspective. Good and bad statistical practices have been presented in an attempt for manufactures to appreciate the risks of using these metrics. Conclusions concerning (1) control charts to be used instead of line/run charts for trend analysis, (2) Ppk as the preferred capability index (but still with an ambition to get processes into statistical control), (3) show process capability indices along with their respective control charts (4) determine which Manufacturing State of Control the product/process lies in (5) an effective Control Strategy can only be implemented if the Manufacturing State of Control is understood, (6) when presenting data consider what is truly representative of the product/process and not the average (7) Management should align with ICH Q10 more effectively to provide statistical resources for their personnel.
机译:适当和不恰当地应用统计指标的影响验证了审计员的观点审查了药物制造的控制状态。已经提出了良好和糟糕的统计实践,以便制造商以欣赏使用这些指标的风险。关于(1)控制图表的结论代替趋势分析的线/运行图表,(2)PPK作为优选的能力指数(但仍然具有将流程的雄心控制到统计控制),(3)显示过程能力指数以及它们各自的控制图(4)确定产品/过程的制造状态在于(5)所在的(5)只有在理解的制造控制状态时才可以实现有效的控制策略,(6)当呈现数据时考虑什么真正代表产品/过程,而不是平均(7)管理应更有效地与ICH Q10对齐,为其人员提供统计资源。

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