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自ISPE第2版出老后,很少提及CCA,不过对于刚涉及到风险评估的小白来说还是要学习的,想请教下各位大佬,对着七条问题是怎么理解的?
1- The component/function is used to demonstrate compliance with theregistered process?
部件/功能是否用于证明符合所注册工艺的规定? 2- The normal operation or control of thecomponent/function has a direct on product quality?
功能/部件的正常操作或控制对产品质量或功效具有直接影响? 3- Failure or alarm of the component/functionwill have a direct effect on product quality or efficacy?
功能/部件的故障或报警是否对产品质量或功效具有直接影响? 4- Information from this component/functionis recorded as part of the batch record, lot release data, or other GMP-relateddocumentation?
从功能/部件获取的信息被记录为批记录、批放行数据或其它GMP相关文件的一部分? 5- The component has direct contact withproduct or product components?
该部件和产品或产品组分有直接接触? 6- The component/function controls criticalprocess elements that may affect product quality, without independentverification of the control system performance?
该部件/功能用于控制可能影响产品质量的关键工艺参数,并且对于控制系统性能没有独立的验证? 7- The component/function is used to create or preserve a criticalstatus of a system?
功能/部件用于创建或保持一个系统的关键状态?
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