be validated for the sterilization process. This features components which include corner protectors, filters and instrument holders or organizers. The design and improvement of a decontamination cycle usually takes place on completion with the OQ. USP3 once again presents guidance on this subject matter as does PIC/S6 which revealed https://medium.com/@tailinscitech/vhp-sterilization-solutions-by-tailin-bioengineering-protecting-pharma-and-laboratory-environments-b515737bff96