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 what contract testing is and the benefits of using contract testing organizations to support you with medical device regulatory testing.
Learn about sterilization by dry heat, how it is performed, and how it can be used to depyrogenate medical devices and products.
Learn about steam sterilization, dry heat sterilization, and which method to use to sterilize various medical devices and products.
Learn about sterilization by dry heat, how is it performed, and when to use it for sterilization of your medical devices and products.
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.