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AI Act QMS:
System Lifecycle Management

Our structured, auditable approach for the full lifecycle of high-risk AI systems

Overview

AI Lifecycle Management requires a structured, auditable approach with support for the full lifecycle of AI systems within the AI Quality Management System. This will ensure that design, development, verification, validation, deployment, and ongoing monitoring activities are conducted in a controlled manner that directly contributes to the protection of health, safety, and fundamental rights of affected persons, achievement of intended purposes and regulatory compliance in alignment with the EU AI Act and EN 18286 requirements.

AI system lifecycle management addresses key AI-specific operational controls by replacing ad-hoc or high-level governance documentation with a dedicated, stage-gated workflow. All stages should be linked to a central AI System Register, risk management processes, and audit programmes, with immutable snapshots taken at critical transition points.

Structured Stages

AI system lifecycle management should be organised into the following sequential, iterative stages. Each stage should comprise defined inputs, activities, outputs, controls, and evidence requirements. Progression between stages should require documented review and approval, with full traceability captured through a universal QMS control feature.

1. Data Preparation

2. Model Development

3. Verification & Validation

4. Deployment

5. Monitoring

Integration with Other Platform Capabilities

The lifecycle management module is deeply integrated with Risk Management, Audit Programmes, Change Management, Evidence Generation, and Nonconformity processes - ensuring end-to-end traceability and protection throughout the AI system's life.

Benefits for Protection of Health, Safety, and Fundamental Rights

This structured approach ensures AI systems are not deployed without rigorous validation, provides regulators with clear evidence, enables proactive issue detection, and supports the EU AI Act's emphasis on technical documentation, human oversight, and post-market monitoring.