Highlights : About MasterControl Risk Analysis
Product Details
Features
Automated task assignment/routing
Best-practice
Corrective actions (CAPA)
Change control
Corrective and preventive action system
Customer complaints software
Customizable reports
Defect tracking
Document approval
Document control
Electronic submissions
Forms-based processes automation
Group sign-off
ISO standards management
Incident management
Nonconformance automation software
Priority levels
Quality audit management
Real-time status
Risk assessment and classification
Benefits
MasterControl enables users to streamline and automate task assignment/routing, scheduling, escalation, tracking, follow-up, review, and approval of all documents-based processes.
The MasterControl CAPA system tracks incidents and guides quality teams through CAPA implementation.
Customizable reports provide users with real-time status reports of the entire quality system, including change control tasks.
MasterControl streamlines complaint-handling with a simple, three-stop process in a pre-configured, multi-page form.
MasterControl facilitates electronic submissions of FDA applications, and provides assembling control and documentation tracking.
MasterControl was the world's first Quality Management System to become CFR 21 Certified. We also offer solutions for FDA, ISO, and Non-regulated/Non-compliance.
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