Quality Excellence
Quality Management System (QMS)
Simplify audits and compliance by digitizing all quality processes. Manage CAPAs, deviations, change controls, and audits in one integrated platform with built-in continuous improvement workflows.
Open CAPAs
12
Audit Score
96%
On-Time Close
98.5%
| Id | Type | Status | Time |
|---|---|---|---|
| CAPA-2024-089 | Corrective | In Progress | 12 days |
| CAPA-2024-088 | Preventive | Closed | - |
Comprehensive Quality Management
Key Features
All quality processes in one integrated system for complete visibility and control.
CAPA Management
End-to-end corrective and preventive action tracking. Root cause analysis tools and effectiveness verification.
Deviation Handling
Capture, investigate, and resolve deviations quickly. Classification, impact assessment, and trending analysis.
Audit Management
Plan, execute, and track internal and external audits. Finding management and follow-up workflows.
Change Control
Structured change management with impact assessment, approvals, and implementation tracking.
Complaint Management
Customer complaint intake, investigation, and resolution. Trend analysis and reporting.
Risk Management
Quality risk assessment and mitigation. Risk registers, FMEA support, and control monitoring.
Investigation
The Investigation component ensures that problems are not guessed, ignored, or temporarily fixed, but logically analyzed and permanently resolved.
Incident
Helps users capture unwanted events early, preventing hidden issues from affecting results and ensuring every decision is based on the right conditions.
OOT-OOC-OOS
Highlights when machine performance starts drifting from historical patterns, even if results look acceptable. Spot hidden shifts early and keep processes stable.
Drive Continuous Improvement
Benefits
Transform quality from a compliance burden into a competitive advantage.
Pass Every Audit
45% Faster CAPA
Proactive Quality
Complete Visibility
Built for Regulated Industries
Regulatory Compliance
Pre-configured for major quality standards with the flexibility to adapt to your specific requirements.
- ISO 9001:2015
- ISO 13485
- FDA 21 CFR Part 820
- GMP/GLP Requirements
- ICH Q10
- EU MDR/IVDR
Plan
Define objectives, metrics, and quality goals
Do
Execute processes and capture data
Check
Monitor, measure, and analyze results
Act
Implement improvements continuously
Ready to Elevate Your Quality Management?
See how Fiscal Ox QMS can transform your quality processes. Schedule a personalized demo today.
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