What is a required practice when preparing compounded sterile preparations?

Ensuring environmental cleanliness is crucial when preparing compounded sterile preparations. This practice helps to minimize the risk of contamination and maintains the integrity of the sterile product. A clean environment, such as a laminar airflow hood or a cleanroom, controls airborne particles and reduces the possibility of microbial growth in the compounded preparation.

In sterile compounding, visual inspections for cleanliness, appropriate cleaning protocols, and proper garbing techniques are essential to ensure that the environment does not contribute to contamination. Such measures are fundamental to safeguarding patient safety by ensuring that the medications administered to patients are free from harmful microorganisms and contaminants. This aligns with regulatory standards set by organizations such as the U.S. Pharmacopeia and the Food and Drug Administration, which emphasize the importance of a sterile environment in the compounding process.