Which of the following is NOT a characteristic of a High Risk CSP?

In the context of compounding sterile preparations, a High Risk Compounding Sterile Preparations (CSP) is defined by specific characteristics that increase the risk of contamination and subsequently the potential for infection when administered to patients. The defining characteristic of High Risk CSPs is their involvement with non-sterile ingredients, as these products can introduce pathogens if not handled under strict aseptic conditions.

When considering the characteristics mentioned:

• The use of sterile products does not define a High Risk CSP; rather, high-risk compounding involves either non-sterile ingredients or handling sterile products in a manner that does not meet stringent standards. Guidelines indicate that if sterile products are used properly and under controlled environments, they are not classified as high risk.

• The presence of non-sterile ingredients is a key factor that raises the risk because it necessitates a requirement for sterilization before patient administration.

• Involvement of bulk drug containers also represents a high-risk situation. These containers can be a source of contamination and require special handling to ensure the integrity of the compounded sterile preparation.

• Lastly, the need for sterilization of end products is a characteristic of High Risk CSPs. This emphasizes that the compounded preparation must be sterile due to the initial introduction of non-