Sterilizer Validation Australia
 
 

Leaders in process
validation and design.

STEAM & h2O2 sTERILIZERS | wASHER dISINFECTORS | eNDOSCOPe reprocessors
Endoscope Storage Cabinets | sTEAM & wATER | hEAT sEALERS
mANUAL pROCESSES | HOSPITAL DESIGN | SPECIALIZED CONSULTANCY

 
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Every process. Fully independent.

SVA is the leading provider of Performance Qualification [PQ] services in Australia.
We work with Health Organisations of all sizes to increase process performance and achieve compliance goals through annual validation studies.

SVA validate all reprocessing equipment found within central sterilizing and endoscopy departments. All manufacturers, all types, all sizes. 100% independent with no product to sell, Australia-wide.

This means that we validate not only a piece of equipment, but entire processes; from transport to decontamination, all the way through to transport back to theatre, and everything in between.

 
 
 
 

Proudly partnering with outstanding healthcare teams for almost twenty years.

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Shine a light.


SVA is passionate about compliant testing.
Our test equipment and methodologies are scrutinized against the specifications
outlined by Standards; down to the last 0.1mm, 0.1°C and 0.1mbar.

That’s because we know that the most challenging parts of a medical device to
clean and sterilize are often the most difficult to reach to test. Without the right equipment,
accurate testing within a fine lumen, a complex hinge or long channel is impossible.

Data too, is only as valuable as it is precise. Our data resolution meets, and in many cases
exceeds the requirements of Standards. Pair this with NATA-traceable calibration protocols
of the highest quality, including on-site oil bath verification, and PQ provides
the line of sight that’s needed to bring confidence to critical processes.



 
 
 

More than 100,000 validation data sets. And counting.

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