What does USP chapter 795 focus on?

USP Chapter 795 specifically addresses the standards and practices surrounding non-sterile compounding of pharmaceutical preparations. This chapter outlines requirements for the compounding process involving non-sterile drugs, providing guidelines to ensure proper practices that lead to quality and safety in the preparation, storage, and dispensing of these products.

The focus on non-sterile compounding includes regulations on the compounding environments, the qualifications of personnel, the necessary equipment, and the documentation required to ensure the compounding process is carried out properly. As a result, pharmacists and pharmacy technicians can create medications tailored to individual patient needs while adhering to quality standards.

In contrast, the other options pertain to different aspects of compounding. Sterile compounding, mentioned in one of the options, is addressed by USP Chapter 797, while hazardous drug compounding is the focus of USP Chapter 800. Pharmaceutical quality assurance might involve several aspects of pharmacy practice but is not the specific focus of USP Chapter 795. Thus, the emphasis on non-sterile compounding makes the chosen answer correct.