设备清洁程序验证中的“注意事项”。

J Agalloco
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引用次数: 0

摘要

在最近的检查中,清洁验证受到了FDA越来越多的关注,但很少有关于制药行业实践的出版物。本报告将回顾设备清洁程序验证的几个方面。介绍的很大一部分来自作者在过去几年中就这一主题所领导的圆桌讨论。要定义的具体领域包括:抽样方法、分析方法、物理参数,以及最重要的可接受标准的选择。本报告还包括一些作者开发的关于清洁验证主题的额外观点,这些观点可能对从业者有用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
"Points to consider" in the validation of equipment cleaning procedures.

Cleaning validation has received increasing attention by the FDA in recent inspections, yet very little has been published regarding practices within the pharmaceutical industry. This presentation will review several of aspects of the validation of equipment cleaning procedures. A significant portion of the presentation is derived from round table discussions the author has led over the last several years on this subject. Specific areas to be defined include: sampling methods, analytical methods, physical parameters, and of greatest interest, the selection of acceptance criteria. The presentation also includes some additional perspectives on the subject of cleaning validation developed by the author which may prove useful to the practitioner.

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