Software Ensures Medical Compliance

American MSI's Celltrack Pro is a production-logging system that enables medical-device makers to comply with the FDA's stringent 21 CFR Part 11 regulations. It can reduce a company's financial exposure by limiting recalls to production batches with specific fail criteria, and it contributes to improved quality through increased visibility of production and employee activities. The supplier says that unlike programs derived from resource planning or production monitoring applications, Celltrack Pro was designed for 21 CFR Part 11 requirements, but it can be used for other markets. American MSI Corp., 5245 Maureen Ln., Moorpark, CA 93021 www.americanmsi.com