What are the compounding standards for sterile and non-sterile preparations?

The correct answer is based on the established standards for compounding practices in pharmacy. The guidelines that govern compounding preparations are outlined by the United States Pharmacopeia (USP). For non-sterile preparations, USP Chapter 795 provides standards that address the compounding of those medications, including aspects such as storage requirements, labeling, and quality control to ensure the safety and efficacy of non-sterile compounded products.

For sterile preparations, USP Chapter 797 details the standards necessary to prevent contamination and ensure the safety and quality of compounded sterile products (CSPs). This chapter includes requirements for the environment in which sterile compounding is performed, personnel training, and procedures to follow to reduce the risk of infection or contamination.

The other choices listed do not correlate with the recognized standards for compounding practices. Therefore, the use of USP Chapters 795 and 797 as the compounding standards for non-sterile and sterile preparations is the foundation for ensuring compliance and safety in pharmaceutical compounding.