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User Manual

EU AI Act Compliance Management System™

Repository: RRVI™

Version: 1.0.2


1. Purpose

This User Manual explains how organizations use the EU AI Act Compliance Management System to establish, maintain and continuously improve compliance with Regulation (EU) 2024/1689.

The manual is intended for organizations acting primarily as AI Deployers.


2. Intended Audience

This manual is intended for:


3. Repository Structure

The repository contains ten compliance modules.

Each module contains seven controlled documents.

Policy Procedure Work Instruction Checklist Register Evidence Declaration

Total:


4. Compliance Lifecycle

The Compliance Management System follows the same lifecycle for every module.

``` Policy ↓

Procedure ↓

Work Instruction ↓

Checklist ↓

Register ↓

Evidence ↓

Declaration ```

Every declaration shall be supported by objective evidence.


5. Getting Started

Before using the Compliance Management System:


6. Completing Module 01 — AI System Inventory

Objective

Identify every AI system used by the organization.

Complete:

The AI Inventory becomes the foundation for every other module.


7. Completing Module 02 — Risk Classification

Objective

Determine the EU AI Act risk category for every AI system.

Update the Risk Classification Register whenever new AI systems are introduced.


8. Completing Module 03 — AI Literacy

Objective

Ensure personnel have sufficient AI Literacy appropriate to their role.

Maintain evidence of completed awareness and training activities.


9. Completing Module 04 — Prohibited Practices

Objective

Verify that no prohibited AI practices are implemented.

Document assessments and retain supporting evidence.


10. Completing Module 05 — High-Risk Assessment

Objective

Determine whether any AI system qualifies as High-Risk under the EU AI Act.

Document conclusions and supporting rationale.


11. Completing Module 06 — Technical Documentation

Objective

Maintain complete technical documentation for applicable AI systems.

Review documentation after significant technical changes.


12. Completing Module 07 — Human Oversight

Objective

Assign responsible human operators and define oversight mechanisms.

Document review, approval and override responsibilities.


13. Completing Module 08 — Data Governance

Objective

Document data sources, ownership, classification and quality.

Review whenever datasets or processing activities change.


14. Completing Module 09 — Logging & Monitoring

Objective

Maintain operational logs and monitoring records.

Ensure logs are protected and retained according to policy.


15. Completing Module 10 — Incident Reporting

Objective

Identify, investigate and resolve AI-related incidents.

Maintain complete incident records and corrective actions.


16. Annual Review

At least once every year:


17. Internal Audit

Use:

Verify that every module remains complete and consistent.


18. Regulatory Inspection

During an inspection:

  1. Present README.md.
  2. Present DOCUMENT_INDEX.md.
  3. Demonstrate each module.
  4. Present Registers.
  5. Present Evidence.
  6. Present Declarations.
  7. Demonstrate traceability.

19. Document Control

Every document shall be:


20. Continuous Improvement

The Compliance Management System shall be updated whenever:


Version

1.0.2

Prepared by

your compliance officer

your organization

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