Sterile Filtration is used to prevent microbial contamination in the pharmaceutical industry. By providing a reliable, safe, and effective way to ensure product manufacturing, the process reduces the risk of microbial contamination in patients. Multiple vendors offer a diverse range of products and formats for a variety of applications. In any pharmaceutical operation, this is the most important filtration process. The United States Food and Drug Administration (USFDA) and the United States Pharmacopoeia (USP) define sterile filtration as a nominal rating of 0.2 m and 0.22 m, respectively, for producing sterile effluent. A sterile filtration step's goal is to remove any viable microorganisms present in the bulk product.
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