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    ISO/IEC 42001

    ISO/IEC 42001 Internal Audit: Building the Evidence Request List Before Fieldwork

    An internal audit of an AI management system succeeds or fails before fieldwork starts, in the evidence request list. A vague list ("please provide your AI governance documentation") produces a folder of policies and a week of follow-up emails. A precise list, where every item names an owner, a period, a source system and the reason it is being asked for, produces evidence that can actually be examined and tested.

    This article provides an original evidence request list for an ISO/IEC 42001:2023 internal audit, explains the four fields every request should carry, and shows how to tell self-reported evidence from inspected and tested evidence when the responses come back.

    By
    AuditPartners
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    Reading time
    10 min
    Status
    Educational guide

    What ISO/IEC 42001 asks of an internal audit

    ISO/IEC 42001:2023 follows the harmonised structure used by other ISO management-system standards such as ISO/IEC 27001:2022: clauses 4 to 10 cover context, leadership, planning, support, operation, performance evaluation and improvement, and Annex A lists control objectives and controls that the organisation selects and justifies in a Statement of Applicability. The internal audit requirement sits in the performance-evaluation clause and expects audits at planned intervals that determine whether the AI management system conforms to the organisation's own requirements and to the standard, and is effectively implemented and maintained.

    The standard's text is licensed and is paraphrased here rather than reproduced. Audit programme design and auditor competence are the subject of ISO 19011; if the audit is performed by an internal audit function, the IIA's Global Internal Audit Standards also apply. Those two sources are not interchangeable, and the audit plan should say which governs.

    The four fields every request needs

    • Owner. The named role that holds the evidence. Not 'the AI team'; the person who can export the record.
    • Period. The date range or point in time the evidence must cover. An audit of a management system that has run for nine months asks for nine months of records, not the latest example.
    • Source. The system of record the evidence comes from: a ticketing tool, a model registry, an IAM console, a board minute book. Naming the source lets the auditor ask for a system export rather than a slide.
    • Purpose. The requirement or control objective the evidence will be compared against, in the organisation's own words. Stating the purpose lets the owner provide the right thing and lets the auditor spot when something else has been substituted.

    A request that lacks any of these will come back as self-report: a description of the process instead of the records that show it ran.

    The evidence request list

    The list below is an original worked example written for a fictional organisation; it is not a reproduction of the standard's clauses or Annex A. The period is the twelve months to 30 September 2026. Sample sizes and periods are illustrative, selected by risk and scope rather than universal requirements. Independent impact-review examples reflect Kestrel's own illustrative organisation criteria, not blanket ISO/IEC 42001 requirements. Adapt owners, sources and purposes to your own management system and Statement of Applicability.

    Evidence request list for the Kestrel Health Analytics ISO/IEC 42001 internal audit (twelve months to 30 September 2026)
    #RequestOwnerPeriodSourcePurpose
    1Current AI management system scope statement and the list of AI systems in scope, with the criteria used to decide inclusion.Head of AI GovernanceAs at 30 Sep 2026Governance repositoryConfirm scope is defined and the three systems are in it; test whether any AI use outside the list should be inside it.
    2AI policy and the record of its approval by top management, including the version history.Head of AI GovernanceOct 2025 – Sep 2026Document management systemLeadership commitment and policy currency; check the approved version is the one staff can access.
    3Roles and responsibilities matrix for AI systems, including named system owners and the person accountable for the AI management system.Chief Risk OfficerAs at 30 Sep 2026Governance repository / HR systemAccountability is assigned to real, current people; cross-check names against the HR leavers list.
    4AI risk assessment methodology and the completed risk assessment for each of the three systems, with risk owner sign-off.AI Risk LeadLatest assessment per system, plus any re-assessment in periodRisk register (GRC tool export)Risk assessment performed per the methodology; impact assessment covers affected individuals and groups, not only the organisation.
    5AI system impact assessments for the clinical summariser and claims classifier, with dates and reviewers.System ownersLatest version in periodGovernance repositoryImpact on individuals and society considered for the higher-risk systems; reviewers independent of the development team under Kestrel's own illustrative criteria, not a blanket requirement of the standard.
    6Statement of Applicability with justification for included and excluded Annex A controls, and its approval record.Head of AI GovernanceCurrent version, with change logGovernance repositoryControl selection is justified and approved; excluded controls have a stated reason.
    7Risk treatment plan with actions, owners, due dates and status, and evidence of closure for any action marked complete.AI Risk LeadOct 2025 – Sep 2026GRC tool export; ticketing systemTreatment is planned and tracked; completed actions have evidence, not just a status change.
    8AI objectives for the year and the measurements reported against them.Head of AI GovernanceFY to 30 Sep 2026Management reporting packObjectives are measurable and were measured; trace one metric to its source data.
    9Competence records for people who develop, deploy and oversee the three systems, including training completion and any competence gaps identified.HR Business PartnerOct 2025 – Sep 2026Learning management systemCompetence is determined and addressed; sample five people across roles.
    10Inventory of data used to train, fine-tune or ground each system, with provenance, consent or lawful basis, and quality checks performed.Data Governance LeadPer system, currentData catalogueData provenance and quality are managed; the free AI System Inventory Template shows the fields we expect.
    11Model and system lifecycle records for the claims classifier: requirements, design decisions, verification and validation results, release approvals.Claims ML LeadAll releases in periodModel registry; CI/CD systemDevelopment follows the defined process; select two releases and trace each from requirement to approval.
    12Change records for every production change to the three systems, including model updates and prompt or configuration changes.Platform Engineering LeadOct 2025 – Sep 2026Change management tool; deployment logsChanges are controlled; reconcile the change list to the deployment log population and sample ten.
    13Operational monitoring outputs: performance, drift and incident indicators for each system, and the review records showing someone looked at them.System ownersMonthly, Oct 2025 – Sep 2026Monitoring platform; review meeting minutesMonitoring is performed and acted on; absence of review records is a finding even if dashboards exist.
    14AI incident and near-miss log, with root-cause analysis and corrective actions for each closed item.AI Risk LeadOct 2025 – Sep 2026Incident management systemIncidents are captured, investigated and lead to corrective action; cross-check against support tickets mentioning model errors.
    15Third-party and supplier records for externally sourced models and AI services, including contracts, due-diligence results and monitoring.Procurement LeadCurrent suppliers plus any onboarded in periodContract repository; vendor risk toolSupplier AI risk is assessed and monitored; see AI Vendor Risk Assessment: Questions to Ask Before You Buy for what due diligence should contain.
    16Communications to affected users and customers about AI use, including any transparency notices and the record of what was published when.Head of ProductOct 2025 – Sep 2026Website change log; customer communications archiveTransparency obligations the organisation set itself are met; compare notices to actual system behaviour.
    17Previous internal audit report, nonconformities raised and evidence of corrective action for each.Head of AI GovernancePrior audit cycleAudit trackerPrior findings are closed with evidence; re-test one closed item.
    18Management review inputs, minutes and resulting decisions and actions.Executive Assistant to the COOAll reviews in periodBoard and executive minute bookTop management reviewed the management system and decided on actions; confirm the inputs the standard expects were actually tabled.
    Item numbering is for the worked example only. Where a request refers to a clause area of ISO/IEC 42001:2023, it does so by subject, not by quoting the clause. The AI Audit Evidence Request Checklist is a downloadable version of this structure with blank result columns.

    When the evidence comes back: self-reported, inspected, tested

    The request list produces inputs. What the auditor does with them determines what the audit can conclude. Using the methods described in NIST SP 800-53A as a vocabulary: interview produces self-reported evidence, examine produces inspected evidence, and test produces tested evidence.

    Three responses to request 13 (operational monitoring) and what each supports
    Response receivedClassificationWhat it supportsWhat it does not support
    The system owner describes the monthly review process in a meeting and says it has happened every month.Self-reportedWhere to look next; the owner's understanding of the process.That any review occurred.
    Twelve monthly review-meeting minutes with attendees, metrics discussed and actions, exported from the minutes tool with creation timestamps.InspectedReliable operating records can support that monthly reviews operated, who attended and what was decided.That the metrics shown were accurate or that actions were completed.
    Auditor re-performs the drift calculation for two months from the monitoring platform's raw data, matches it to the minutes, and traces two resulting actions to closed tickets.TestedThat the reviewed figures were correct for the sample and that actions were taken.Anything about the ten months not re-performed; conclusions are limited to the sample.

    Gaps this list tends to surface

    • Named owners who have left the organisation (request 3 against the leavers list).
    • Impact assessments with no independent reviewer where the organisation's own criteria require one (request 5 in this fictional example, not a blanket ISO/IEC 42001 requirement).
    • Risk treatment actions marked complete with no closure evidence (request 7).
    • Prompt and configuration changes that bypass change management because they are not 'code' (request 12).
    • Dashboards that exist but were never reviewed, with no minutes or actions (request 13).
    • Supplier models in production with no due-diligence record because they were onboarded by a product team through a credit card (request 15).

    If you are not yet at the point of an internal audit, the free AI Governance QuickScan covers basic inventory, ownership and policy themes at a preliminary, self-reported level in under ten minutes; it does not cover the evidence request list. When you are ready to plan an audit or a pre-certification gap assessment, our Framework Assessments & Internal Audits page describes how we scope the work.

    Key takeaways

    • Every evidence request needs an owner, a period, a source system and a purpose; without them you receive descriptions, not records.
    • Ask for populations over the audit period, then sample; the latest example proves only that one example exists.
    • Classify what comes back as self-reported, inspected or tested, and write conclusions that name their basis.
    • ISO/IEC 42001:2023 is licensed; request by subject and your own Statement of Applicability, not by copying clause text.
    • An internal audit is an input to certification, never a certificate.
    Related serviceFramework AssessmentsRelated resourceAI Audit Evidence Request ChecklistFree toolAI Governance QuickScan

    References

    Primary sources cited above. Standards are referenced by number and year; their text is licensed and is paraphrased, not reproduced.

    1. ISO/IEC 42001:2023, Artificial intelligence management system — Requirements (opens in a new tab) — Licensed text; structure and requirements paraphrased.
    2. ISO/IEC 27001:2022, Information security management systems — Requirements (opens in a new tab) — Harmonised structure shared with ISO/IEC 42001.
    3. ISO 19011, Guidelines for auditing management systems (opens in a new tab) — Audit programme and auditor competence guidance.
    4. The IIA, Global Internal Audit Standards (effective 9 January 2025) (opens in a new tab)
    5. NIST SP 800-53A Rev. 5, Assessing Security and Privacy Controls, January 2022 (opens in a new tab) — Examine, interview and test methods.
    6. NIST AI 100-1, AI Risk Management Framework (AI RMF 1.0), January 2023 (opens in a new tab) — Risk and impact assessment practices that many AI management systems adopt as their methodology.

    Need this applied to your environment?

    A scoped assessment follows the agreed criteria, procedures and evidence described here. Findings are reviewed and signed off by accountable professionals.