Managing the risks inherent in nonsterile compounding requires a comprehensive pharmacy compliance program that incorporates established USP 795 standards into daily practice
A closed-loop solution that supports efforts to comply with USP Chapter 795 is essential for ensuring patient safety and the overall quality of medications compounded.
What is USP 795?
USP Chapter 795 compounding non-sterile preparations pertains to extemporaneous compounding of pharmaceuticals, which is an integral pharmacy operation, especially in community pharmacies and pediatric hospitals.
Errors and health and safety risks are inherent in nonsterile compounding. USP guidelines for 795 were developed to address specific areas of pharmacy responsibility, including:
- Staff competency
- Ingredient quality
- Equipment maintenance and use
- Process standardization
- Safe and appropriate environment
- Inspection and documentation
- Accurate Beyond-Use dating (BUD)
How Simplifi 797 streamlines USP 795 compliance in your pharmacy
Simplifi® 797 is a closed-loop, expert-developed web-based solution that supports compliance with USP 795 in the pharmacy. The solution includes: