Bacterial Endotoxin vs. Bioburden Testing
Learn about the differences between bioburden, bacterial endotoxins, and their medical device testing methods.
Learn about the differences between bioburden, bacterial endotoxins, and their medical device testing methods.
What is antimicrobial activity for medical products and why it is important for bioburden testing. Learn how to neutralize it for regulatory testing.
Microorganism recovery efficiency is essential for bioburden test validity. Learn more about product sample preparation and microorganism recovery.
Learn about the examination methods and techniques covered in USP 61 and how these relate to bioburden testing.
What is bacterial endotoxin testing? Why are endotoxins harmful? Learn about it and how bacterial endotoxin testing is performed.
Learn about the U.S. Pharmacopeia and the differences between USP 60, USP 61, and USP 62 standards.
Learn all about the methods covered in USP 60 and how these relate to bioburden testing.
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.
Appropriate decontamination processes for medical devices must occur to prevent the transmission of disease, especially for reusable devices reprocessed by health care facilities.