Incubation &
Reporting Options
for Single Kits

Aseptic
Technique
Kits

Quality
Assurance
Management

Total CSP
Quality
Management

Facility
USP <797>
Compliance

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.

Where do I begin?

Learn how to establish a verification program, design a CSP facility, implement USP <797>, and much more.

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Achieve NIOSH Compliance

Safe Compounding of Hazardous Drugs Manual

ChemoTEQ™ Hazardous Compounding Aseptic Technique Verification Kit

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>.