Equipment set up and qualification ought to be carried out per the maker’s instructions. A prerequisite to qualifying the equipment will be the qualification of any utilities supporting the equipment. The design and development of the decontamination cycle typically takes place on completion from the OQ. USP3 yet again https://tailinscitech.wixsite.com/tailinscitech/post/optimizing-pharma-filling-and-sealing-processes-with-tailin-technology