USP Chapter 800 enforcement is approaching – are you prepared?
Take the stress out of hazardous drug compounding. Simplifi 797 is a comprehensive web-based quality management system that helps meet the requirements of both USP Chapters <795>, <797> and <800> for compounding medications. This turnkey, yet flexible solution scales to the needs of your facilities.
Only focusing on hazardous drug compounding? Our USP 800 Module provides the tools needed to comply with USP Chapter <800>, improve patient and staff safety and mitigate risk when compounding hazardous drugs.
Simplifi 797 offers turnkey compliance through customizable tasks, real-time alerts on compliance risks, advanced analytics, observational competency evaluations, staff training, and policies & procedures – allowing for streamlined pharmacy operations and compliance that can be centrally managed from anywhere.
“Simplifi 797 provides the tools and resources needed to ensure compliance with hazardous compounding standards mandated by USP Chapter <800>. The updated policies and procedures, competency assessments and facility-specific formulary are key to helping your cleanroom mitigate the risks from hazardous drug compounding.”
– Eric S. Kastango, MBA, BSPharm, FASHP
Using Simplifi 797 enables your compounding staff to manage USP 800 compliance:
Additional Simplifi 797 features addressing USP <800> requirements enable staff to:
Take the first steps toward compliance with USP 797 standards
Accuracy of CSPs and ensuring a state of control are both needed in a cleanroom