Sterile compounding is a highly specialized area of pharmaceutical practice dedicated to preparing medications free from microbial contamination and particulates. It is guided by strict regulatory frameworks, such as USP <797>, which establishes standards to ensure the safety, sterility, and efficacy of compounded sterile preparations (CSPs). This article explores the procedures, challenges, and testing methods involved in sterile compounding, focusing on stability testing, degradation risks, and the benefits of terminal sterilization to extend Beyond-Use Dates (BUDs). Read More >