Validation Services for Sterilizers

Compulsory every 12 months according to AS/NZS 4815:2006.

The Validation process, also called Performance Qualification, includes calibration and chamber profiling as well as further testing to ensure that your sterilizer  is capable of sterilizing the most challenging load that you process in your practice.

Validation also requires the completion of Biological Indicator Testing. This is easy to do by practice staff, and MDSNQ will provide instructions and support although we recommend testing be performed in conjunction with your Pathology Service provider.

The RACGP Infection Control Standards state that microbiological qualification is to be performed by the member of staff with designated responsibility for sterilization. This is why MDSNQ staff do not perform this testing, but support you through the process. 

Our Validation Sterilizer Service includes:

• A heat distribution test - chamber profiling 
• Penetration Time/Time at Temperature Test Report
• Maintenance as required
• Detailed instructions and support for the completion of Biological Indicator Testing in conjunction with your Pathology Service provider

If required our maintenance services include, but are not limited to:

• Adjusting and lubricating hinges
• Replacing wear-and-tear parts such as door seals and air filters
• Checking and cleaning where required 
• General maintenance assessment