What is a key requirement for environments where sterile preparations are compounded?

A key requirement for environments where sterile preparations are compounded is maintaining an ISO class 5 or better classification. This specifies that the air cleanliness level in the compounding area must have a maximum allowable particle count of less than 3,520 particles per cubic meter of air that are 0.5 micrometers or larger. ISO class 5 ensures that the environment is sufficiently clean to minimize the risk of contamination during the preparation of sterile products, protecting patient safety and ensuring the efficacy of the compounded medications.

While controlled lighting, frequent cleaning, and low traffic can all contribute to maintaining a sterile environment, they do not specifically address the air quality and contamination control requirements mandated by ISO standards. The focus on ISO classifications exists to standardize and regulate the compounding environments, which is crucial for facilities involved in sterile compounding practices.