Our testing assesses the compatibility of medical devices with biological systems
We provide tests to help you validate your sterilization process in accordance with international standards.
We provide validation to sterilization dose for you to achieve a sterile label claim product.
Our endotoxin test is used to predict the release of harmful endotoxins from medical device
Periodic monitoring is needed to ensure working environment is in a good condition
The microflora of your product provides information on contamination sources and elimination methods
We offers variations of bioburden test methods to suit customers' requirements through our accredited in-house method
