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    Chapter III · High-risk AI systems

    Article 17 — Quality management system

    Provider

    What the article requiresUnder review

    1. 01Put a quality management system in place, documented in written policies, procedures and instructions, and proportionate to the size of the organisation.
    2. 02Set out a strategy for regulatory compliance, including compliance with conformity assessment procedures and procedures for managing modifications.
    3. 03Control the design, design verification and the design control of the system.
    4. 04Control development, quality control and quality assurance.
    5. 05Define examination, test and validation procedures, and how often they are carried out.
    6. 06Identify the technical specifications and standards applied, and, where harmonised standards are not applied in full, the means used to meet the requirements.
    7. 07Operate systems and procedures for data management, covering acquisition, collection, analysis, labelling, storage, filtration, mining, aggregation and retention.
    8. 08Operate the risk management system of Article 9.
    9. 09Set up and operate a post-market monitoring system under Article 72.
    10. 10Operate procedures for reporting serious incidents under Article 73.
    11. 11Handle communication with competent authorities, notified bodies, customers and other operators.
    12. 12Keep records of all relevant documentation and information.
    13. 13Manage resources, including security-of-supply measures.
    14. 14Define an accountability framework setting out the responsibilities of management and staff.

    In practiceUnder review

    Article 17 is the first AI Act article with a published European standard: EN 18286, available from CEN-CENELEC since 22 July 2026. Inclusiveness Newsletter, Edition 16, reports that its reference has not been published in the Official Journal. That makes Article 17 a practical starting point for structured quality-management documentation. Requirement modelling for Article 17 is available on request; it restates the Article 17 duties, does not reproduce EN 18286 and is not a clause-by-clause mapping of the standard.

    Standards addressing this articleUnder review

    Training and practical application

    In-house training on building and documenting a quality management system under Article 17 with EN 18286. Training is not certification.

    View the EN 18286 course →

    VocabularyUnder review

    Source: Regulation (EU) 2024/1689, as amended by Regulation (EU) 2026/1744. EUR-Lex.

    Summaries and role mappings are editorial work by Georg Philip Krog. Only the Official Journal text is authentic.