Process Validation
Accurate and calibrated medical equipment validation, available for all brands and models.
- Washer-Disinfectors, Autoclaves, Bedpan Washers, Sterilisers, Laboratory Washers, Utensil Washers, Robotic Automation and CSSD equipment.
- Ultrasonic Cleaners, Operating Tables, Blanket Warmers, Endoscope Washers, Reverse Osmosis Systems, Steam Generators and Boilers.
Annual validation of sterilization and washer-disinfector processes is required by AS 5369 (formerly AS/NZS 4187) for Reprocessing of Reusable Medical Devices and health policies.
We Offer
- Device qualification covering performance and operation.
- Timestamped cycle logs for accreditation audits and compliance.
- Secure remote monitoring for auditing and troubleshooting.
- Expert guidance on corrective actions to exceed regulatory thresholds.
Why Regular Validation Matters
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.