Sterilization Vs. Pasteurization For Parenteral Products
Learn the differences between pasteurization and sterilization, the benefits of pasteurization and the requirements for sterilization validation.
Learn the differences between pasteurization and sterilization, the benefits of pasteurization and the requirements for sterilization validation.
Learn how particular matter testing is performed and how this relates to regulatory requirements for therapeutic protein injections.
Learn the differences between traditional particulate matter testing and particulate matter testing for biologics for therapeutic protein products.
Learn how particular matter testing is performed, which method to use, and how this relates to regulatory requirements for injectable parenteral products.
Learn how particulate matter testing is performed and how this microbiology test relates to regulatory requirements for ophthalmic solutions.
Learn about the issues with electronic particle counters and what to watch out for with light obscuration particle count testing for parenteral products.
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.
Learn about endogenous and exogenous pyrogens and how they relate to regulatory requirements for your medical devices and products.
Learn about the methods used after initial manufacturing and after stability testing to test for the sterility of your medical device or product.