Accurate medical equipment validation services available.
Validation activities follow AS 5369 for Reprocessing of Reusable Medical Devices. Where applicable, we reference AS ISO 15883 for washer-disinfectors, AS ISO 17665 for moist heat sterilization, and AS NZS 3551 for medical equipment management programs.
Annual validation of sterilization and washer-disinfector processes is required by AS 5369 and jurisdictional health policies. Our documentation and traceability support accreditation and regulatory obligations.
Engage our experts to conduct annual validation for every medical device under your care.
Documented inspections and calibration create full visibility of asset condition. Reports include photographic records of critical components, calibration certificates, and trend summaries that support evidence-based decisions.
Performance data highlights early degradation, so maintenance intervals can be tuned to reduce reactive callouts and extend asset life by up to 30 percent, and reduce total lifecycle cost.
Our programme ensures full compliance with National Safety and Quality Health Service Standard 3 (NSQHS) on Preventing and Controlling Infections and supports accreditation audits by generating complete records of all maintenance activities.
A data-driven validation schedule keeps medical assets reliable, compliant, and ready for audits while safeguarding patient safety and operational continuity.
“very happy with the level of service and now have far less breakdowns”