be validated for the sterilization process. This features equipment for example corner protectors, filters and instrument holders or organizers. The design and advancement of the decontamination cycle usually takes place upon completion with the OQ. USP3 once more gives guidance on this topic as does PIC/S6 which released a https://tailinscitech.wordpress.com/2026/02/09/vhp-sterilization-solutions-by-tailin-bioengineering-protecting-pharma-and-laboratory-environments/