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Platform Solution

Quality Management System

Document control, NCR management, and corrective actions aligned with ISO/IEC 17025, 17020, and ISO 9001 clause structure.

Solution · Platform Module

OMS QMS provides a fully integrated quality management system covering document control, non-conformance recording, corrective and preventive actions, internal audit management, and management review — all linked to your live job and test records.

Every quality event is timestamped, user-attributed, and clause-referenced against your applicable standard. NCRs link directly to the job, asset, or personnel record that triggered them — giving auditors a single, traceable chain from root cause to verified closure.

QMS documents are version-controlled with approval workflows, ensuring only authorised releases are in use at any time. The system supports multi-site labs, with configurable access controls per branch or department.

What It Does

Key Capabilities

Version-controlled document library with approval and release workflows
NCR logging with root cause analysis fields and objective evidence attachments
CAPAR tracking from initiation through to verified closure
Internal audit scheduling, checklists, and finding management
Management review records with action tracking
Clause-mapped compliance registers for ISO/IEC 17025, 17020, ISO 9001
Corrective action due-date alerts and escalation notifications

Standards Coverage

Applicable Standards

ISO/IEC 17025ISO/IEC 17020ISO 9001:2015IATF 16949AS 9100 Rev DAPI Q1/Q2

Ready to see Quality Management System in action?

Join accredited laboratories and inspection bodies already using OMS Software to manage compliance, workflows, and reporting.

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