In today’s regulatory markets it is absolutely essential that your manufacturing inspection systems have the necessary audit logs, calibration records, and security properties.

With QCIS^TM, the power of compliance is at your finger tips. QCIS^TM facilitates Medical Device and Pharmaceutical manufacturers to meet GMP and obtain 21 CFR Part 11 Compliance.

QCIS^TM instantly gives you control of your inspection system’s configuration management,  custom reports, audit trail history, product traceability, and operator management.

In addition to data management, with QCIS^TM you can enforce regular schedule calibrations and track calibration events in a simple report.

Operator Management

• Custom Permission Level
• Password Management
• Create & Modify Operators 
• Operator Groups
• Operator Certification

• Audit Trails
• Configuration Reports
• Result Reports
• Printing Reports
• Remote Access

• Operator Lockout
• Calibration Lockout
• Custom Reports
• Instrument Configuration
• Database Backups

Audit Trail History for System Configuration, Operator Management, Calibration History.