Practical guide / United Kingdom

How to conduct an ISO 27001 internal audit: a seven-step method with templates

The seven steps of a Clause 9.2 internal audit, each with its inputs, outputs and a realistic time range, a one-page sample audit plan, one piece of evidence graded three ways, the report structure section by section, and a downloadable report template.

The company, people and records in the examples are fictional learning aids, not client results. Buy ISO/IEC 27001:2022 and ISO 19011:2018 for the normative text.

Before you start: what an internal audit has to achieve

An ISO 27001 internal audit has one job, set by Clause 9.2 of ISO/IEC 27001:2022: provide information on whether the information security management system conforms to the organisation’s own requirements and to the standard, and whether it is effectively implemented and maintained. The seven steps below are the method Aegentra uses on outsourced audits for UK organisations, written out so that an internal team can run the same process. Each step names its inputs, its output and a realistic time range for a single-site organisation of up to about one hundred people. Larger scopes scale the sampling and interview days, not the method.

If you need the requirement itself explained first, read the Clause 9.2 requirements guide. If you want the audit done by an independent auditor, the ISO 27001 internal audit service page describes the same seven steps as a fixed-fee engagement from £1,500 + VAT.

The seven steps, with inputs, outputs and time

  1. Scope and plan the audit

    Time half a day to one dayInputs audit programme, ISMS scope statement, Statement of Applicability, previous audit report, organisation chartOutput a written audit plan

    Start from the audit programme, not from a checklist. Confirm which clauses and which applicable Annex A controls this audit covers, which sites, systems and teams are in scope, and which period of records you will sample. Write the criteria explicitly: the clause numbers, the control references from the SoA, and the organisation’s own policies and procedures you will test against.

    Record the auditor’s competence and independence in the plan. If the auditor had any part in designing or operating a control in scope, exclude that control from their work or assign it to someone else. Agree evidence access and confidentiality with the ISMS owner, and send interview requests with the topics listed so people arrive with the right records.

  2. Review the documented information

    Time one to two daysInputs policies, procedures, risk assessment and treatment plan, SoA, objectives, audit programme, management-review minutes, previous findingsOutput an evidence request list and a question set per area

    Read the ISMS documents against the criteria before you speak to anyone. The purpose is not to grade the writing; it is to learn what the organisation has committed to, so that interviews and sampling can test whether those commitments are kept. Note every place where a procedure sets a specific obligation (a timeframe, an approval, a review period, a record to be kept): each is a testable criterion.

    Build the evidence request list from those obligations. For a leaver procedure that requires access removal within one working day, the request is the leaver population for the period and the access-removal records for a sample. For a supplier security policy that requires annual review, the request is the supplier register and the review records.

  3. Interview control owners

    Time one to two daysInputs question set, evidence request list, access to the people who run each processOutput interview notes referenced to criteria

    Interview the people who operate the controls, not only the ISMS manager. Ask how the process actually runs, what happens when it does not, and what records exist. Listen for the difference between what the procedure says and what is done. Where someone describes a record, ask to see it during the interview rather than accepting the description; this is the single habit that most improves audit quality.

    Keep notes that reference the criterion each answer relates to. Interview evidence is useful for understanding and for finding where to sample; on its own it rarely supports a conclusion about effectiveness.

  4. Select the sample and test the evidence

    Time one to three daysInputs the complete population behind each control (leavers, changes, incidents, supplier reviews, access reviews), the records for the sampled itemsOutput evidence references and test results

    Reconcile the population first. If the leaver list comes from HR and the access-removal tickets from IT, compare them before sampling, because the gap between the two is often the finding. Choose a sample that is justified in writing: risk, volume, change and previous results drive the size, not a fixed percentage. For a small UK organisation, a sample of five to ten items per control is common; the rationale matters more than the number.

    Test each sampled item against its criterion and record the identifier, the date, the evidence source, the result and any limitation (for example, a record that could not be located). Minimise personal data in the working papers: a ticket number and a date are enough.

  5. Evaluate and grade the findings

    Time half a day to one dayInputs test results, interview notes, the criteriaOutput findings written as criterion, evidence, condition and conclusion

    A finding is only a finding when it is tied to a criterion and supported by evidence. Separate a missing record from a control that did not operate: an unlocated access review may mean the review was not done, or that it was done and not filed, and the two have different causes and different gradings. Put every potential nonconformity back to the control owner before you grade it, and record the response. Findings that are withdrawn on evidence are reported as such, not dropped.

    Grade consistently. A major nonconformity is a requirement not met in a way that undermines the ISMS or a control’s ability to achieve its intended outcome, or a pattern of minors. A minor nonconformity is a single lapse against a requirement. An opportunity for improvement is a requirement that is met but could be met better. An observation is a matter to watch. The sample finding below shows the same evidence written at three gradings.

  6. Write and present the report

    Time one dayInputs findings, plan, working-paper indexOutput the audit report, presented at a closing meeting

    Write for two readers: management, who will act on it at management review, and the certification auditor, who will read it as evidence under Clause 9.2. State the objectives, scope and criteria; the methods used and the sample sizes; each finding with its grading; the limitations of the audit; and a conclusion on conformity and effectiveness for the scope audited. Keep the working papers indexed so any conclusion can be traced back to the evidence.

    Hold a closing meeting. Walk through every finding, confirm the facts are accepted, and agree who owns each action. The report template in the download section follows this structure section by section.

  7. Follow up corrective action

    Time spread across the following weeksInputs the action record, closure evidence from control ownersOutput verified closures, inputs to management review and to the next audit programme

    Management owns correction and corrective action under Clause 10.2: fix the immediate issue, find the cause, act on the cause, and check that the action worked. The auditor’s role is to verify closure on evidence, not to accept a ticket marked done. Agree in advance who verifies and when, feed the status into management review under Clause 9.3, and let the results shape the frequency and coverage of the next cycle in the programme, which is what Clause 9.2.2 asks for.

A sample audit plan

This is the plan for a fictional UK software company, forty staff, one office, production hosted in a public cloud, certified to ISO/IEC 27001:2022 and nine weeks from its first surveillance audit. It fits on one page, which is the right length.

Plan elementEntry
Audit objectiveDetermine whether the ISMS conforms to ISO/IEC 27001:2022 and to the organisation’s own requirements, and whether it is effectively implemented and maintained, for the scope below.
ScopeThe ISMS as defined in the scope statement v2.1: the hosted platform, its development and support, the London office and remote workers. Records from 1 April to 30 September.
CriteriaISO/IEC 27001:2022 Clauses 4 to 10; Annex A controls marked applicable in SoA v3.0 and selected for this cycle (see coverage); ISMS policies P01 to P14; supplier contract clauses for the two hosting providers.
Coverage this cycleAll of Clauses 4 to 10. Annex A: 5.1, 5.9, 5.15, 5.18, 5.19, 5.23, 5.24, 5.26, 6.1, 6.3, 6.5, 7.7, 7.10, 8.1, 8.2, 8.5, 8.8, 8.9, 8.13, 8.15, 8.16, 8.24, 8.25, 8.32. Remaining applicable controls scheduled for cycle two per the programme.
MethodsDocument review; interviews with the CTO, head of engineering, people lead, IT lead and support lead; sampling of leavers, joiners, changes, incidents, access reviews, supplier reviews and backups; remote inspection of cloud and identity configuration; one on-site visit for physical controls.
Auditor and independenceNamed auditor, ISO 27001 Lead Auditor trained, no role in designing or operating the ISMS; competence record ref C-07; impartiality assessment ref I-02 signed by the managing director.
SchedulePlanning and document review week 1; interviews and sampling weeks 2 and 3; closing meeting end of week 3; report within five working days; verification of closures within six weeks.
Evidence handlingRead-only access to the ticketing system and identity console for the audit period; exports held in the auditor’s encrypted workspace and deleted thirty days after report acceptance; no personal data copied beyond identifiers.
ReportingReport to the managing director and CTO; tabled at the October management review; made available to the certification body.

One piece of evidence, written three ways

Grading is where internal audits most often go wrong, in both directions: lapses written up as majors because the auditor wants to be taken seriously, and genuine nonconformities softened into observations because the control owner is a colleague. The same evidence, graded against the same criterion, should read differently only because the condition differs. Here is one leaver-handling test written at three gradings.

Observation
All eight sampled leavers had access removed within the required time. In two cases the removal was completed by the IT lead from a personal reminder rather than from a ticket, so the control depends on one person’s diligence rather than on the process. No requirement is breached. Recommend that HR’s leaver notification create the IT ticket automatically.
Minor nonconformity
Seven of eight sampled leavers had access removed within the required time. One contractor’s account (ticket 4821) remained enabled for six working days after the last working day recorded by HR; the console log shows no sign-in during that period. Requirement P07 section 4.2 was not met for this item. Cause reported by the IT lead: the contractor was not on the HR leaver list because contractors are managed by the engineering lead. Corrective action required on the population, not only the account.
Major nonconformity
Four of eight sampled leavers retained access beyond the required time, by between three and forty-one working days, and one account (ticket 4790) was used to sign in nine days after the leaver’s last day. The contractor population is not covered by the leaver process at all, and no access review in the period detected the retained accounts (Annex A 5.18). Requirement P07 section 4.2 is not met as a process, and the control is not achieving its intended outcome. Immediate correction of the open accounts, investigation of the post-leaving sign-in under the incident procedure, and corrective action on the process and the access review are required before the surveillance audit.

Notice what changes: the condition observed, the proportion of the sample affected, whether the cause is an individual lapse or a process gap, and whether a related control that should have caught it also failed. Notice what does not change: the criterion is quoted, the sample is stated, each item is identified by a reference rather than a name, and the conclusion stays within what the evidence supports.

What the audit report contains, section by section

The report is the deliverable the certification body reads and the document management acts on. The structure below is the one used in the downloadable template.

SectionContentsWhy it is there
1. SummaryOne paragraph: scope, dates, auditor, number of findings by grade, overall conclusion on conformity and effectiveness.Management reads this; the certification auditor starts here.
2. Objectives, scope and criteriaCopied from the audit plan, with any changes made during fieldwork and why.Clause 9.2.2 requires defined criteria and scope; the report proves they were used.
3. Methods and samplingMethods per area; population and sample size per control tested; how samples were selected.Lets a reader judge the weight of each conclusion.
4. LimitationsEvidence not available, areas not reached, remote versus on-site coverage.An audit that claims no limitations is not believed.
5. FindingsEach finding as criterion, evidence, condition, conclusion and grading, with a reference number and the control owner.Clause 10.2 corrective action starts from here.
6. Matters examined and closedPotential nonconformities raised in fieldwork and closed on evidence, with the reasoning.Transparency; it also shows the audit tested its own findings.
7. Verification of previous findingsStatus of each finding from the previous internal and external audits.Certification bodies check that earlier findings were closed effectively.
8. ConclusionWhether the ISMS, for the scope audited, conforms and is effectively implemented and maintained, with any qualifications.This is the “information” Clause 9.2.1 asks the audit to provide.
9. Action recordFinding reference, owner, correction, corrective action, due date, verification method and status.Feeds management review and the next audit programme.
AppendixWorking-paper index: interviews, documents reviewed, samples and evidence references.Traceability from every conclusion back to evidence.

Six mistakes that turn an internal audit into a certification finding

  • Auditing the documents and calling it an audit of the ISMS. Clause 9.2.1 asks whether the system is effectively implemented and maintained. That needs operating records and people, not policies alone.
  • Sampling without a population. Picking the five best-documented changes tells you nothing. Get the full list first, then sample from it with a stated rationale.
  • Letting the ISMS owner audit their own work. It fails the objectivity requirement in 9.2.2 and it is the first thing a certification auditor checks.
  • Writing “compliant” with no evidence reference. A conclusion with no trail to a sample is an opinion. Index the working papers.
  • Grading every lapse the same. A missing record, a single lapse and a failed process are three different findings with three different corrective actions.
  • Finishing the audit after the certification body arrives. The report has to be tabled at management review and available as evidence before the external audit, or it has done half its job.

Downloads

ISO 27001 internal audit report template (DOCX)

Word document · the nine sections above plus the working-paper index · UK English

Download the report template

ISO 27001 internal audit plan and checklist template (CSV)

Opens in Excel or Google Sheets · Clauses 4 to 10 and Annex A sample tests · criterion, population, method and findings columns

Download the plan and checklist template

Templates are starting points. The agreed scope, criteria and sample decide the content of a real audit.

Questions readers ask.

How long does an ISO 27001 internal audit take?

For a single-site UK organisation of up to about a hundred people with one clear ISMS scope, plan for five to ten auditor days spread over three to four weeks: roughly one day of planning, one to two of document review, one to two of interviews, one to three of sampling and testing, one of evaluation and one of reporting, with follow-up verification afterwards. Multiple sites, a wide Annex A sample or poor evidence access extend the sampling and interview days.

Who should conduct the internal audit?

Someone competent in ISO 27001 and in auditing who had no part in designing or operating the controls they audit. That can be an employee from another function with training and documented independence, an auditor exchanged with a peer organisation, or an outsourced provider. The organisation must record the competence and impartiality assessment whichever route it takes.

What should an ISO 27001 internal audit report contain?

A summary; the objectives, scope and criteria; the methods and sample sizes; the limitations; each finding written as criterion, evidence, condition, conclusion and grading; matters examined and closed; verification of previous findings; a conclusion on conformity and effectiveness; and an action record with owners and dates. An appendix should index the working papers.

How do I choose a sample size for an internal audit?

Start from the full population for the control and the period, then choose a sample whose size and selection you can justify in writing: higher risk, higher volume, recent change and previous findings all argue for more items. For many controls in a small organisation, five to ten items selected across the period, including any known exceptions, is defensible. Record the rationale in the plan and the report.

What is the difference between a nonconformity, an opportunity for improvement and an observation?

A nonconformity is a requirement of the standard or of the organisation’s own ISMS that is not fulfilled, graded major when it undermines the ISMS or a control’s intended outcome and minor when it is a single lapse. An opportunity for improvement is a requirement that is met but could be met better; it needs no corrective action. An observation is a matter noted for attention, such as an emerging risk or a recent change.

Can we use the checklist as the audit?

No. A checklist is a planning aid that lists what to look at. The audit is the evidence you gather against each item, the sample you justify, the interviews you hold and the conclusion you write. A completed checklist with ticks and no evidence references does not meet Clause 9.2 and will not satisfy a certification body.

Does the audit need to be finished before the certification body visits?

Yes, in practice. The certification auditor expects to see a current internal audit report, the findings tracked into corrective action and the report tabled at management review. Schedule the internal audit to complete at least a month before the surveillance or recertification audit so closures can be verified.

What if we find a serious problem during the internal audit?

Report it immediately to the ISMS owner rather than waiting for the closing meeting, so correction can start. If it is also a security incident, it goes through the incident procedure as well as the audit. Grade it honestly in the report; a major nonconformity found and acted on internally is a far better position at the external audit than one found by the certification body.

Choose the next step.