It is a microbiological analysis performed after the production of medical devices and before the sterilization process. With this analysis, it is carried out to calculate the total biological load on the medical device during the production phase and to determine the total number of viable microorganisms. The purpose of this analysis is to help manufacturers determine the effective sterilization process.
Bioburden Tests are carried out in our laboratory as accredited according to ISO 11737-1 standard.
