On-site validation
Testing and validation conducted in accordance with AS 5369:2023, applicable procedures and the manufacturer’s instructions.
Validation & testing
Evidence you can trust. Confidence in every cycle.
Professional on-site validation and testing for most autoclave brands, with methodical assessment and clear documentation to help your practice demonstrate safe, consistent performance.
Book validationWhy validation matters
Protect people. Support compliance. Prove performance.
Fantastic Medical provides validation services for most autoclave brands to help confirm that your equipment and sterilisation process continue to perform safely and consistently.
Keeping validation current supports your obligations under AS 5369:2023 and applicable manufacturer requirements, while helping safeguard your staff, clients and patients. Scope and frequency are confirmed for your equipment, load configuration and practice requirements.
What’s included
A complete, clearly documented validation service.
Testing is carried out on site and tailored to the autoclave, its intended use and the challenge loads processed by your practice.
Chamber temperature mapping
Independent measurement across the chamber to assess temperature distribution and identify cold spots or inconsistent conditions.
Performance Qualification (PQ)
Validation cycles performed with representative challenge loads, including independent temperature and pressure measurement.
Biological indicator testing
Biological indicators used where applicable to provide microbiological evidence of sterilisation process effectiveness.
Validation identification
A validation sticker is affixed to the autoclave, recording the validation date and helping your team see its current status.
Comprehensive digital report
A professionally prepared digital report brings the test scope, results and findings together in an easy-to-store, share and retrieve format for your records and audit preparation.
Clear evidence, practical support
More than a test result.
We explain the outcome in plain language and identify any observations or follow-up actions. Our reminder service contacts you approximately one month before your next validation is due, helping you plan ahead and keep records current.
Reminder timing is approximate and should support—not replace—your practice’s own compliance calendar.Ready to get started?