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The demonstration ought to be carried out the water system is generating the demanded quality and quantity of water whilst operated according to the pertinent SOP.

根据 cGMP 的要求，需要对制造设施进行适当的设计。确保它们遵守当地法规以及药品制造法规。

A cleaning validation protocol shall be formulated for your ‘worst circumstance’ product selected for your cleaning validation method. Adhering to information (although not limited to) the subsequent included in the cleaning validation protocol.

To make certain the product could be properly transported in just the required temperature profile Which compliance with regulatory requirements plus the anticipations of intrigued events might be shown:

工艺验证是一个循序渐进的过程，旨在确保制造工艺能够始终如一地生产出优质产品。它由制药行业制造商的质量保证负责人领导的验证团队执行。尽管严格意义上的工艺验证包括工艺设计的阶段，但在实际操作中，工艺验证通常是在发布新产品之前进行的。在开始时建立的工艺验证协议（validation protocol）应明确规定如何执行验证过程，包括要监控的参数、要采集的样本和接受的结果标准。需要注意的是，在商业化生产之前，制造商应该确认产品能够满足所需的质量标准，并且设计的生产工艺满足安全性和有效性相关的要求。

I would love to enroll in newsletters from Sartorius (Sartorius AG and its affiliated corporations) based of my personalized interests.

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持续工艺验证涉及在商业产品生产过程中的持续验证，以确保在先前阶段设计和确认的工艺能够按照期待的那样继续提供一致的产品质量。这是一个生命周期管理（lifecycle management）的范畴。

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The acceptance criteria read more with the cleaning validation will probably be mentioned in the specific protocol and will determine based upon the solution matrix.

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