ISO27K

ISO 27001 checklist, clause by clause

A checklist made of clause headings tells you nothing about whether you are ready. This one follows the order the work actually happens in, and every item says what done looks like and what the audit team will ask you to produce.

Last reviewed 2026-09-15Written by Jacob Masse, TrazTech Inc.

ISO/IEC 27001:2022 has two halves that behave differently. Clauses 4 to 10 carry 25 mandatory requirements, none excludable. Annex A lists 93 reference controls, and which of those apply is an output of your risk treatment rather than an input to it. Ticking all 93 before doing a risk assessment produces a Statement of Applicability nobody can defend.

The order below is the dependency order. Scope constrains the risk assessment, the assessment produces the treatment plan, the plan decides Annex A, and the rest is evidence that the system is running. The requirements are set out clause by clause on the clauses page, and the route to a certificate here is on ISO 27001 certification in Canada.

25 Mandatory requirements in clauses 4 to 10, none excludable

93 Annex A reference controls, applicability decided by risk

2 Audit stages before a certificate is issued

Each item below names an artifact, the condition that makes it done, and the question asked about it in the audit room. An item is not done because a document exists. It is done when the document is approved, dated, owned by somebody who can explain it, and matched by what happens in the business.

Clause 4: context and scope

A scope written too wide drags systems, offices and teams into an audit that did not need to be there. One written too narrow gets challenged at stage 1, or satisfies nobody in your pipeline because the certificate does not cover the product the customer buys.

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What a certification auditor looks for in clause 4

Evidence that passes. A documented scope statement naming the organization units, locations, systems and interfaces inside the ISMS, a record of internal and external issues, and a list of interested parties with their requirements. Stage 1 reads these first.

How long. One to three weeks. The scope decision is the one that sets the cost of everything after it.

Common mistakes. A scope so narrow buyers will not accept it, or so wide the company cannot run it; interested parties listed with no requirements; and interfaces to out-of-scope systems left undescribed.

Canadian note. List the regulators that apply to you as interested parties: the Privacy Commissioner of Canada under PIPEDA, the Commission d'accès à l'information for Quebec personal information, and any sector regulator such as OSFI if you serve federally regulated financial institutions.

Clause 5: leadership

Clause 5 asks for three things and auditors test them by talking to people rather than reading documents. The evidence is whether the answers match.

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What a certification auditor looks for in clause 5

Evidence that passes. A signed information security policy, documented roles and responsibilities, and minutes or emails showing top management actually made decisions about the ISMS. Auditors interview a senior leader during Stage 2.

How long. A week to draft and approve. The evidence of commitment builds over the months before the audit.

Common mistakes. A leader who cannot say what the ISMS is for in the interview, and a policy approved by the person who wrote it rather than by top management.

Tip. Put ISMS decisions on an existing leadership meeting agenda each quarter. Two lines of minutes each time is better evidence than a single long annual review.

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Clause 6: planning, risk and the Statement of Applicability

This is the largest block of work and it determines everything downstream. Do it in the stated order: a risk assessment run before the methodology is agreed produces results nobody can reproduce, and reproducibility is an explicit requirement.

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What a certification auditor looks for in clause 6

Evidence that passes. A risk assessment method, a risk register with owners and treatment decisions, a risk treatment plan, measurable security objectives, and a Statement of Applicability covering all 93 Annex A controls with a justification for every inclusion and exclusion.

How long. Three to six weeks for a first risk assessment and Statement of Applicability. It is the largest single piece of work before Stage 1.

Common mistakes. A Statement of Applicability that excludes controls without a reason, risk owners who do not know they are risk owners, and objectives nobody measures.

2022 note. Certificates to the 2013 edition had to transition by October 31, 2025, so every audit now uses the 2022 control set. The 2024 amendment also asks you to consider whether climate change is a relevant issue in clauses 4.1 and 4.2.

The ordering trap

If your Statement of Applicability was produced by opening Annex A and marking almost everything applicable, the audit team can see it: the justifications read as generic and no control traces back to a risk. Letting the register drive control selection saves an argument at every audit that follows.

Clause 7: support

Clause 7 separates a system that exists on paper from one people use. Four of its five requirements are about human beings.

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What a certification auditor looks for in clause 7

Evidence that passes. Competence records for people with ISMS roles, awareness training completion for everyone in scope, a communication plan, and document control showing versions, approvals and where the current copy lives.

How long. Two to four weeks to set up training and document control. Competence records are often the slowest part because they need CVs, certificates or training records per role.

Common mistakes. Training assigned but not completed, several versions of the same policy in circulation, and competence claimed for roles with no record behind it.

Canadian note. Where training covers personal information handling, align it with your PIPEDA and Law 25 obligations so the same record serves both.

Clause 8: operation

Clause 8 is short in the standard and long in practice. Run the processes you designed and keep the evidence that you ran them.

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What a certification auditor looks for in clause 8

Evidence that passes. Evidence that the risk treatment plan is being carried out: controls implemented, changes managed, suppliers assessed, and a risk assessment repeated when something significant changed.

How long. This is the operating period. Most certification bodies want to see the ISMS running for about three months before Stage 2.

Common mistakes. Treating the risk assessment as a one-off document, and supplier assessments that stop at collecting a certificate without checking what scope it covers.

Tip. Keep a simple log of significant changes and whether each triggered a risk review. Auditors ask for it, and it is easy to keep and hard to reconstruct.

Clause 9: performance evaluation

Three requirements, and the last two are the ones a certification body checks have genuinely happened before it will issue anything.

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What a certification auditor looks for in clause 9

Evidence that passes. Monitoring results against your objectives, a completed internal audit program with findings, and a management review that covers every input clause 9.3 lists, with decisions recorded.

How long. An internal audit of a small ISMS takes two to five days. A management review is a two-hour meeting with a prepared pack.

Common mistakes. An internal audit done by the person who built the ISMS, a management review that skips required inputs, and metrics with no targets.

Independence. The internal auditor must be objective and impartial. A small company can use a colleague from another function, or bring in an outside auditor for a few days.

Clause 10: improvement

Two requirements, and an empty nonconformity log is itself a signal.

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What a certification auditor looks for in clause 10

Evidence that passes. A nonconformity and corrective action log with root causes, the action taken and a check that it worked, plus examples of improvement you made on your own initiative.

How long. Ongoing. The log should have entries before Stage 2, usually from the internal audit.

Common mistakes. An empty log, which looks like nobody is looking, and corrective actions closed without checking they fixed the cause.

After certification. Surveillance audits happen each year and recertification every three years. The corrective action log is the first thing a surveillance auditor opens.

Annex A: 93 controls in four themes

Annex A of the 2022 edition holds 93 controls in four themes. The 2013 edition had 114 in 14 domains and nothing was removed in the rewrite. Controls were merged and regrouped by who owns them.

Annex A themes in ISO/IEC 27001:2022 and what each covers
ThemeControlsWhat it covers
Organizational37Policies, roles, supplier and cloud relationships, threat intelligence, incident management, continuity, legal requirements
People8Screening, terms of employment, awareness, disciplinary process, duties after termination, remote working, reporting events
Physical14Perimeters, entry, secure areas, equipment siting, cabling, maintenance, secure disposal, clear desk and screen
Technological34Endpoints, privileged access, cryptography, secure development, logging, monitoring, backup, data masking, web filtering
Total reference controls93Applicability decided by risk treatment

The checklist item here is not "implement 93 controls". It is that every control has a recorded decision, every applicable control traces to a risk or a requirement and carries a status and an owner, and every exclusion has a justification that would survive being read aloud. Excluding a control because you have no on-premises data centre is defensible. Excluding one because it looked difficult is a finding waiting to happen, and the physical controls are where that shows up in remote-first companies that still keep an office.

The Annex A controls page sets out what each theme expects, and the Annex A control selector gives a first pass at applicability. Implementation guidance lives in ISO 27002, which is not itself certifiable.

Before the certification audit

Certification runs in two stages with the same audit team. Stage 1 reads, stage 2 tests, and knowing which questions belong to which stage is the difference between a clean pass and findings that delay the certificate.

What each audit stage asks for
Stage 1, documentation reviewStage 2, effectiveness audit
Scope statement, and whether it matches what you sellInterviews to see whether the documented process is the one staff follow
Information security policy and supporting policiesSamples of records across the period: access reviews, change approvals, incident tickets
Risk methodology, risk assessment and treatment planEvidence that treatment actions were implemented on the dates claimed
Statement of Applicability, including exclusionsControl testing against the applicable controls in the Statement of Applicability
Internal audit plan and reportsWhether findings raised internally were actually closed
Management review minutesWhether decisions recorded in the review led to anything
Readiness for stage 2, and a dateNonconformities, graded major or minor, with a window to respond

The gap between stages runs from a few weeks to a few months, and a stage 1 finding that the system has not operated long enough is the usual cause of the longer gap. Evidence samples need three months of operation at the short end. The stage 1 and stage 2 page covers what happens between them, the stage 1 readiness check flags what is missing before you book a date, and a gap assessment does the same job against a longer runway.

The items that fail most often

  1. Interfaces and dependencies missing from clause 4, which makes the scope unverifiable.
  2. A Statement of Applicability where applicable controls trace to no risk.
  3. Objectives that are not measurable, so clause 9 has nothing to measure against.
  4. Internal audit performed by the person who built the system, failing the independence requirement.
  5. Management review minutes missing two or three of the required inputs.
  6. Corrective actions closed without an effectiveness review.
  7. Awareness records covering employees but not contractors.

Each is cheaper to fix before stage 1 than after stage 2. The free tools on this site ask for no email address.

What to do next

This month. Settle scope and write the risk method. They drive every other clause.

Next. Run the risk assessment and draft the Statement of Applicability against the 93 Annex A controls, with a reason for every exclusion.

Before Stage 1. Operate the ISMS for about three months, complete an internal audit and a management review, and log the corrective actions.

Choosing a certification body. Use one accredited for ISO 27001 by an IAF member, such as the Standards Council of Canada, and check the accreditation on the IAF CertSearch database. Ask for Stage 1 and Stage 2 dates in writing.

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Common questions

Do we have to implement all 93 Annex A controls?

No. You have to make and record a decision about all 93. Which ones apply is determined by your risk treatment and by legal, regulatory and contractual requirements, and the Statement of Applicability is where those decisions are written down. Most organizations end up with a large majority applicable, but each exclusion has to rest on a reason that relates to your situation.

Can we do the internal audit ourselves?

Yes, as long as the auditor is independent of the work being audited. In a small company that means somebody from a different function, or an outside party. The person who wrote the policies and built the controls cannot audit them, and that is the most common way this requirement fails. Keep a record of the auditor's training or experience.

How long does the checklist take to work through?

For a company under 100 people starting from documented but informal practice, six to nine months to stage 2 is realistic, and the binding constraint is elapsed time rather than effort. Clause 9 needs an internal audit and a management review to have happened, and clause 8 needs operating history. Neither compresses by adding people.

This directory is published by TrazTech Inc.