Final answer:
A quality assurance program in sterile compounding pharmacies should monitor equipment calibration and maintenance, proper labeling of medications, adherence to sterile compounding guidelines, monitoring of environmental factors, evaluation of raw materials, and training of staff.
Step-by-step explanation:
A quality assurance program in sterile compounding pharmacies should monitor several elements to ensure safety and efficacy. These elements include: Equipment calibration and maintenance to ensure accurate and precise dispensing of medications. Proper labeling of medications to prevent medication errors and ensure patient safety. Adherence to sterile compounding guidelines and procedures to minimize the risk of contamination.
Monitoring of environmental factors such as temperature and humidity to maintain the integrity and stability of medications. Evaluation of the quality and purity of raw materials used in compounding medications. Regular training and education of staff to ensure up-to-date knowledge and competency in sterile compounding practices.