Art. 13(3) mandates that providers supply specific instructions with every high-risk AI system. Without this document, a system cannot legally be placed on the EU market. It is also required content for EU database registration (Annex VIII).
- 1Identify provider and system details
- 2Document intended purpose, capabilities, and performance levels
- 3Specify accuracy metrics, known limitations, and failure modes
- 4Define human oversight measures and technical requirements
- 5Describe logging capabilities and retention periods
- 6Export and include with every deployment of the system
- Art. 13
- Art. 13(3)
- Annex IV §1
Instructions for Use Generator
Mandatory under Art. 13(3) EU AI Act. Fill in the narrative fields plus the structured performance, misuse and input-data sections before exporting.
Provider Identity & Contact
Art. 13(3)(a)
System Identification
Art. 13(3)(b)
Intended Purpose
Art. 13(3)(c)
Capabilities & Limitations
Art. 13(3)(d)
Human Oversight Measures
Art. 13(3)(e)
Technical Measures & Hardware
Art. 13(3)(f)
Logging & Audit Trail
Art. 13(3)(g)
Expected Lifetime & Updates
Art. 13(3)(h)
Performance Levels & Accuracy
Art. 13(3)(b)(ii) / Art. 13(3)(d)(i)
Each row captures one performance metric with its value, the test conditions, the demographic split and the confidence interval. Minimum one row required to export.
Reasonably Foreseeable Misuse
Art. 13(3)(d)(ii)
Tick every category that applies. The "Other" row captures misuse that does not fit the standard taxonomy. At least one category must be selected to export.
Input Data Specification
Art. 13(3)(d)(iii)
Specifications of the input data the system requires and what the system will reject.
Export blocked. 7 required fields missing: AI system name, Version, Provider identity, +4 more
Important Legal Disclaimer
This tool is a self-assessment aid only and does not constitute legal advice, a formally certified compliance assessment, or an independently audited report.
Outputs — including reports, scores, checklists, and generated documents — are for internal use and should be reviewed by a qualified legal representative or independent AI compliance auditor before being relied upon for regulatory, procurement, or public-disclosure purposes.
This tool does not replace a notified body conformity assessment where one is required under Art. 43(1) of the EU AI Act (e.g. biometric identification systems for law enforcement).
All assessment risk lies with the user. AIAuditRef, its developers, and staff accept no liability for losses arising from use of or reliance on these outputs. Always verify against official sources: the EU AI Act (Regulation 2024/1689) and your national enforcement authority.