SPC Charts
Monitor process stability and capability with statistical process control charts that visualize production data in real time. Detect trends, shifts, and out-of-control conditions early using industry-standard control chart methods and Western Electric rules.
Key Capabilities
What you get with the SPC Charts module.
See Document Control & Quality in action
Watch how MoniDoseQMS handles document control & quality workflows end-to-end.
Getting Started
Build your own QMS
Register an account and assemble your quality system from only the modules you need — set up in minutes, with no implementation fee.
Getting Started
Platform tour
A guided tour of MoniDoseQMS after you log in — your profile, the everyday tools (notifications, recycle bin, tasks, events, regulatory news), and the dashboard.
How It Connects
SPC Chartsdoesn't work in isolation. It connects seamlessly with other modules in MoniDoseQMS for full traceability across your quality system.
Ready to see SPC Charts in action?
Book a 30-minute demo tailored to your regulatory needs. Our team will walk you through how SPC Charts works within your specific compliance context.
More in Document Control & Quality
Explore other modules in the Document Control & Quality category.
Document Management Hub
Centralize all quality documents in a single, secure hub with powerful search, categorization, and lifecycle management. Ensure every team member always accesses the latest approved version while maintaining full traceability across your entire document ecosystem.
Document Control
Manage the entire lifecycle of quality documents with version control, electronic signatures, and automated workflows. Ensure every SOP, work instruction, and form meets regulatory requirements with a fully auditable document management system built for regulated industries.
SOP Template Library
Accelerate SOP creation with a curated library of industry-standard templates designed for regulated environments. Reduce drafting time and ensure consistency across your organization with templates aligned to ISO 13485, EU MDR, and FDA requirements.
CAPA Management
Track and manage all corrective and preventive actions with built-in root cause analysis tools. Ensure every CAPA follows a structured workflow from identification through effectiveness verification, with full audit trail and regulatory-ready documentation.
Preventive Actions
Proactively identify and eliminate potential quality problems before they occur. Systematically analyze trends, near-misses, and risk indicators to implement preventive measures that strengthen your quality system and reduce costly corrective actions.
Deviation Management
Capture, investigate, and resolve deviations from established procedures with a structured workflow that ensures nothing falls through the cracks. Classify deviations by severity, conduct thorough investigations, and drive timely resolution with full regulatory traceability.