for Single Kits
Complete, Closed-Loop, Quality Management System for Compounded Sterile Products
Proper use of the VALITEQ® compounding validation systems assures quality management of your CSP programs in accordance with USP <797>. Our pharmacy-friendly systems produce the outcomes necessary to demonstrate continuous quality improvement and assurance of your CSP programs and activities. By standardizing your CSP activities, you will improve the morale of your operatives and simplify your routine quality data acquisition tasks.
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Achieve NIOSH Compliance
Incubation & Reporting Services
Incubation and reporting services are available for all Valiteq hazardous compounding aseptic technique verification kits. Simply return the completed testing cultures in our specially-designed return containers for complete development and reporting, to be used as evidence of compliance with USP <797>.