What is one of the components that a non-sterile compounding policy and procedures manual must include?

A non-sterile compounding policy and procedures manual is essential for ensuring that compounding is done safely, consistently, and in compliance with relevant regulations. One of the crucial components of this manual is environmental quality and control. This aspect includes guidelines on maintaining appropriate cleanliness, temperature, humidity, and overall conditions in the compounding area, which are vital for ensuring the quality and safety of compounded medications.

Proper environmental quality and control help prevent contamination and ensure that non-sterile compounds meet the necessary standards for potency and purity. It outlines the necessary practices and monitoring processes to create a suitable environment for compounding, which is critical to patient safety and the effectiveness of the medication produced.

The other options, while potentially relevant to pharmacy operations in a broader context, do not directly pertain to the essential components of a non-sterile compounding policy. Staff payment structure, marketing strategies, and social media guidelines do not encompass the specific controls and protocols needed to ensure the safe and effective compounding of non-sterile products.