USP3 and PIC/S5 list supplemental items for being concluded while in the OQ which includes cleaning and leak tests. Decontamination cycle progress takes place once the completion with the OQ and is mentioned in detail in part six. It is important to note that regulatory requirements will vary according https://www.tumblr.com/tailinscitech/805885788785180672/optimizing-pharma-filling-and-sealing-processes?source=share