Which of the following is NOT a type of sterile compounding facility?

A non-sterile laboratory is characterized by conditions that do not meet the strict requirements needed for sterile compounding. Sterile compounding requires environments that minimize the risk of contamination, such as controlled airflow and specific cleanliness levels, which are not present in non-sterile settings.

In contrast, an ISO 5 environment represents a controlled area that maintains a specific level of cleanliness to ensure that the air quality, temperature, and humidity are suitable for sterile compounding. Hospital pharmacies may have designated sterile compounding areas equipped to meet regulatory standards, and compounding pharmacies are designed specifically for the preparation of sterile products. Thus, the non-sterile laboratory stands out as not being a facility capable of performing sterile compounding due to its inherent lack of sterile conditions.