How To Perform USP 51 Antimicrobial Testing
Learn how to perform USP 51 antimicrobial testing, what types of product need it, and how it relates to FDA testing for parenteral products.
Learn how to perform USP 51 antimicrobial testing, what types of product need it, and how it relates to FDA testing for parenteral products.
Learn what cleaning validation is and the top three cleaning processes that must be validated to keep your medical device or medical product sterile.
Learn about water sampling and when to use these methods for environmental monitoring of your parenteral products.
Learn the differences between sterilization, sanitization and disinfection, and how they relate to your medical devices and products.
Learn how parametric release programs compare to sterility testing and which option is best to meet regulatory requirements for medical devices or products.
Learn about the challenges that companies face when manufacturing viscous medical and cosmetic products and how to overcome filling them.
Learn about sterile filling and its importance, and how to choose the best method to fill vials and syringes with your parenteral or cosmetic products.
Learn about stability data requirements by FDA development phase for various types of sterile medical devices, products and cosmetics.
Learn what parametric release testing is and how it is related to regulatory requirements during manufacturing process for your medical device or product.
Learn the top ten reasons why prefilled syringes are the top growing parenteral product on the market today!