Animal Health Solutions

Q3 2021

Animal Health Solution - a Covetrus magazine for veterinary professionals

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11 Q3 2021 | Animal Health Solutions There are many types of compounding pharmacies, so how does a veterinarian identify quality when choosing a compounding pharmacy to work with? The laws and regulations that vary by state make it difficult to establish a universal benchmark of quality for veterinary compounding; however, there are things clinicians and veterinary practices can look for to find a trustworthy pharmacy or compounding partner. In this article, which is the third in a series of four, a basic overview of the United States Pharmacopeia (USP) guidelines compounding pharmacies must meet to produce safe, effective, and consistent compounds will be discussed. USP quality compounding components Most quality components are based on human compounding laws, USP standards, and best practices. This is how the current compounding system operates, regardless of patient species. Accreditation through the Pharmacy Compounding Accreditation Board (PCAB) is the only compounding-specific credential available for pharmacies. 1 If a compounding pharmacy is PCAB-accredited, which is usually noted on the pharmacy's website, the pharmacy voluntarily adheres to a comprehensive set of nationally recognized standards for the compounding pharmacy industry. For more on accreditation, please refer to the previous article on compounding regulations at cliniciansbrief.com/article/navigating-compounding-regulations-what- veterinary-community-needs-know. USP monographs The USP is the repository for many monographs involving chemicals used in contemporary compounding. Led by the USP compounding expert committee, the USP publishes compounded preparation monographs, scientifically backed formulations with ingredients, compounding directions, stability data, and packaging/storage recommendations for a specific compound. 5,6 USP monographs can be of particular use in veterinary compounding, in which dozens of compounds are available but are dose-, route-, and ingredient-specific. Further, the USP publishes studies of failed compounded formulations to help avoid the creation of poor preparations. 7

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