Validation & Qualification Portal
Centralized tracking for cross-divisional product validation, vendor qualification, and regulatory compliance workflows. Step 7 in the Enterprise Quality Lifecycle.
1
Initiation
2
Scoping
3
Documentation
4
Testing
5
Review
6
Approval
7
Validation & Qualification
Track Submission
Active Workflow| Component / Division | Standard | Validator | Status | Last Updated |
|---|---|---|---|---|
| Aerospace Propulsion Module | DO-178C / AS9100 | Zenth Aerospace QA | Qualified | 2026-05-18 |
| Quantum Computing Array | ISO 17025 | Aevum Tech Labs | In Validation | 2026-05-20 |
| Medical Imaging Sensor | ISO 13485 / FDA 510(k) | Zenth Health Sciences | Pending Review | 2026-05-22 |
| Autonomous Fleet Controller | ISO 26262 / SOTIF | Aevum Robotics | Qualified | 2026-05-19 |
Qualification Checklist
3 Pending-
Technical Specification Alignment Verified against divisional engineering baselines.
-
Environmental Stress Screening Thermal, vibration, and electromagnetic compatibility passed.
-
Cross-Division Integration Test Requires coordination with Logistics & Digital Systems.
-
Regulatory Compliance Sign-off Pending final audit from Zenth Compliance Office.
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Final Qualification Certificate Issuance Triggered after all validation gates are cleared.
Active Certifications & Standards
ISO 9001:2015
Quality Management
ISO 17025
Testing & Calibration
AS9100 Rev D
Aerospace QMS
ISO 13485
Medical Devices
IEC 61508
Functional Safety
ISO 14001
Environmental Mgmt
Submit for Validation
Upload documentation or request qualification review for new components, vendors, or processes.
Need help with qualification criteria?📞 Validation Support
\nFor urgent qualification blocks or compliance escalations, contact the Zenth Quality Office.
🔒 Secure Portal: az-qms.secure