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01 AUDIT READINESS

Audit Week
Should Feel Like
Any Other Week.

Centralize SOPs, CAPAs, training, deviations, and document control in one intelligent platform. Stay audit-ready, every day.

Always Audit Ready

Real-time readiness across all areas

Complete Traceability

Every action captured, every time

AI-Powered Insights

Spot gaps, risks & trends before they matter

Secure & Compliant

21 CFR Part 11, GxP and more

Overview
Documents
Training
CAPA
Deviations
Change
Reports
Settings
Quality Operations Overview
All systems in control. You are audit-ready.
All Sites ▾
🔔3
Audit Readiness
100%
✓ Ready
SOP Compliance
100%
✓ Compliant
Training Compliance
98.6%
✓ Compliant
Open CAPAs
2
◆ Low Priority
Overdue Items
0
✓ None
Audit Readiness Breakdown
0%
Audit Ready
✓Document Control100%
✓Training98.6%
✓CAPA100%
✓Change Control100%
✓Deviations100%
✓Supplier Quality100%
✓Risk Management100%
Document Control View All
Total Documents
1,247
+12 this month
Approved
1,205
Effective
1,198
Under Review
23
DOC
SOP-GLP-001
Sample Management SOP
EffectiveMay 12, 2025
PDF
WI-PRD-045
Equipment Cleaning Procedure
EffectiveMay 11, 2025
XLS
FRM-QA-102
Batch Record Review Form
Under ReviewMay 10, 2025
PDF
POL-QMS-007
Quality Policy
EffectiveMay 9, 2025
Your organization is fully prepared for any audit, at any time.
FDA21 CFR Part 11
ISOISO 13485
GxPCompliant
Electronic SignaturesCompliant
Audit TrailsComplete
Data IntegrityALCOA+
Global ReadyMulti-Site