Bioburden Testing For Medical Devices
What is bioburden testing? Why is bioburden testing necessary? Learn more about these questions, about bioburden testing methods and more.
What is bioburden testing? Why is bioburden testing necessary? Learn more about these questions, about bioburden testing methods and more.
USP 62 covers tests for specific microorganisms. Learn about the procedures, tests and methods covered in USP 62 and how these relate to bioburden testing.
Looking to determine if your reusable device’s cleaning protocol is robust enough? Use these 6 soil markers to test the cleanliness of your devices.
Learn more about packaging options, packaging material types, and additional packaging considerations for your device.
These are the five calculations you should know related to EO and ECH toxicity limits your product needs to meet.
Learn all about the overkill method and why it is better for you to use it for sterilization validation process of your products.
If you are in need of EO Residual Testing, these are five things you should know about extraction techniques for EO residuals testing.
These are three factors that will effect the EO residual levels of your product following EO sterilization.
Appropriate decontamination processes for medical devices must occur to prevent the transmission of disease, especially for reusable devices reprocessed by health care facilities.
If you are in need of EO Residual Testing, these are the three toxicity limits your product needs to meet.