How to depyrogenate sterile products by rinsing
Learn what depyrogenation by rinsing is, why is depyrogenation needed and how to use rinsing for a medical device’s or product’s endotoxin removal.
Learn what depyrogenation by rinsing is, why is depyrogenation needed and how to use rinsing for a medical device’s or product’s endotoxin removal.
Learn how to select and create endotoxin indicators for depyrogenation validation processes and regulatory testing.
Learn about biological indicators used in sterilization validations and endotoxin indicators for depyrogenation validations.
Learn about the relationship between endotoxins and lipopolysaccharides (LPS), and their similarities and differences.
Learn about sterilization by dry heat, how it is performed, and how it can be used to depyrogenate medical devices and products.
Learn about the differences between bacterial endotoxin testing and environmental monitoring for your medical device or medical product.
Learn techniques for controlling endotoxins in parenteral products so that medical devices, products, and injectables meet FDA limits for pyrogenicity.
Learn about bacterial endotoxins, other pyrogens, and bacterial endotoxin pyrogenicity testing for your medical device or medical product.
Learn techniques for measuring endotoxins during manufacturing to ensure your medical devices, products, and injectables meet FDA limits for pyrogenicity.
Learn how USP 151 pyrogen testing using rabbits is performed and how this relates to regulatory requirements for your medical devices and products.