be validated to the sterilization process. This contains equipment which include corner protectors, filters and instrument holders or organizers. The design and growth of the decontamination cycle normally takes place on completion from the OQ. USP3 once again offers steering on this subject as does PIC/S6 which published a https://tailinscitech.mystrikingly.com/blog/vhp-sterilization-solutions-by-tailin-bioengineering-protecting-pharmaand