VaultISO 27001ISO 27001 mandatory documents: the complete 2022 list
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ISO 27001 mandatory documents: the complete 2022 list

ISO 27001 mandatory documents and records

Harry WestFounder & CEO28 August 20239 min read
Inside This Article
What are the ISO 27001 mandatory documents?Which documents do ISO 27001 clauses 4 to 10 require?Which records does ISO 27001 require you to keep?Which Annex A controls usually need documents?How much ISO 27001 documentation is enough?How do you keep ISO 27001 documents audit-ready?Frequently asked questions
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Key takeaways

ISO 27001 mandatory documents are a short list from clauses 4 to 10: scope, policy, risk processes, Statement of Applicability, treatment plan and objectives, plus records proving the ISMS runs. Annex A documents become expected only for controls your Statement of Applicability marks applicable. Enough documentation is whatever lets every sampled process be shown working.

Core documents
The ISMS scope, information security policy, risk assessment and treatment processes, Statement of Applicability, risk treatment plan and security objectives, all written, approved and kept current under Clause 7.5.
Mandatory records
Competence evidence, risk assessment and treatment results, monitoring results, the audit programme and its results, management review results, and nonconformity and corrective action records, produced as the ISMS operates.
Annex A documents
No Annex A control is mandatory, so neither is its paperwork. Once the Statement of Applicability marks a control applicable, auditors usually expect written rules or procedures behind it.
How much is enough
Clause 7.5 adds whatever your ISMS genuinely needs written down. A procedure you never follow is worse than none, because the auditor will test it and record the gap.

The Stage 1 auditor's first request is your document set. The folder you inherited holds dozens of files of uncertain status, and nobody can say which ones the standard actually requires. This guide lists the ISO 27001 mandatory documents and records clause by clause, separates them from the Annex A documents your Statement of Applicability adds, and shows how much is enough. It is written for security and compliance leads at UK firms of 25–250 people preparing for ISO 27001:2022 certification.

The mandatory core is shorter than most template packs suggest. Most of it is records your management system produces as it runs, not documents you sit down to write.

What are the ISO 27001 mandatory documents?

ISO 27001 mandatory documents are the documented information that clauses 4 to 10 explicitly require: the ISMS scope, the security policy, the risk assessment and treatment processes, the Statement of Applicability, the treatment plan and the objectives. Mandatory records sit alongside them, proving the system ran: competence, risk results, monitoring, audits, reviews and corrective actions.

The ISO/IEC 27001:2022 standard folds both kinds into a single term, documented information. In practice it helps to split documented information by what each piece is for. ISO 27001 sets no document hierarchy, but auditors recognise this working model:

TypeWhat it answersWho approves itHow it changesExample from the mandatory list
PolicyWhat we commit to, and whyTop managementRarely; reviewed at planned intervalsInformation security policy (Clause 5.2)
Topic-specific policy or standardThe rules for one areaThe area's owner, under the main policyWhen the risk or technology changesAccess control rules (A.5.15)
ProcessWhat happens, in what order, with what inputs and outputsThe process ownerWhen the way of working changesRisk assessment process (Clause 6.1.2)
ProcedureStep by step, how one task is doneThe team that does the workOften; kept close to the workIncident response procedure (A.5.26)
PlanWhat we will do, by when, and who owns itThe accountable ownerAs actions closeRisk treatment plan (Clause 6.1.3)
RecordEvidence of what actually happenedNobody; it is produced, not approvedNever edited, only added toInternal audit results (Clause 9.2)

The first five state how you intend to work, so you write, approve and update them. Records are different: the ISMS produces them as it runs, and you keep them unchanged as evidence. ISO's management-system vocabulary describes a policy as top management's formally expressed intentions and direction, and a process as connected activities that turn inputs into outputs. A procedure is narrower: the specified way to carry out one activity.

Most firms over-write procedures and under-produce records. The auditor samples the records.

There is a third category, and it is the one teams forget. Clause 7.5 also covers any documented information you decide the ISMS needs to work, beyond what the standard names. That decision is yours, which is why the right answer differs between a 40-person software firm and a 200-person insurer.

The clause-required list below is the floor. Everything else is either a consequence of your Annex A choices or a judgement about what your people need written down.

Which documents do ISO 27001 clauses 4 to 10 require?

Clauses 4 to 10 require a core set of documents you write and keep current: the ISMS scope, the information security policy, the risk assessment process, the risk treatment process, the Statement of Applicability, the risk treatment plan and the security objectives. Clause 8.1 adds whatever operational information shows your processes run as planned.

Expect the Stage 1 auditor to read each of these before sampling anything else.

ClauseDocumentWhat the auditor checks
4.3ISMS scope statementEntities, services, locations and systems covered; a written case for each exclusion; approval and version
5.2Information security policyLeadership approval, the commitments the clause names, communication to staff, availability to interested parties where appropriate
6.1.2Risk assessment processScales, criteria and an acceptance line that give comparable results every time
6.1.3Risk treatment processHow treatment options are chosen and controls selected, then compared with Annex A
6.1.3Statement of ApplicabilityEvery Annex A control, whether it applies, the reason, and its implementation status
6.1.3Risk treatment planTreatments with named owners and dates, and risk owners' approval of the plan and the residual risk
6.2Information security objectivesMeasurable objectives, each with an owner, resources, a deadline and an evaluation method
8.1Operational planning informationEnough to give confidence that security processes ran as planned

Three of these deserve more attention than the rest.

The Statement of Applicability, risk register and treatment plan must tell one story. Auditors cross-check them against each other faster than internal reviews do. A control marked "implemented" in the Statement of Applicability needs a risk it treats and a trail showing it happened.

A Statement of Applicability that disagrees with your risk register isn't a summary. It's a finding waiting to be written.

The policy is one document, not twenty. Clause 5.2 asks for a single information security policy owned by top management. The topic-specific policies on access, cryptography or acceptable use come from Annex A, which is a different question covered below.

The scope is a commercial document. Buyers read the scope wording on your certificate to learn what it covers. The Clause 4.3 guide covers how to draw that boundary.

One recent change touches the context clauses. ISO/IEC 27001:2022 Amendment 1, published in 2024, asks you to determine whether climate change is a relevant issue. It does not add a named document, but we recommend recording the decision and its reasoning alongside your context analysis, so the auditor can see it was made.

Which records does ISO 27001 require you to keep?

ISO 27001 requires records proving the ISMS operates: evidence of competence, the results of risk assessments and risk treatment, monitoring and measurement results, the internal audit programme and its results, management review results, and records of nonconformities and corrective actions. You add new records over time rather than editing old ones.

ClauseRecordWhat good looks like
7.2Evidence of competenceA role matrix with required skills and current state, plus dated training and certification records
8.2Risk assessment resultsA register with dated passes on schedule and after significant change, each risk with an owner
8.3Risk treatment resultsProof treatments were carried out: configuration exports, tickets, signed risk acceptances
9.1Monitoring and measurement resultsA retained series of metric results, with the evaluation and decisions that followed
9.2Audit programme and audit resultsThe schedule, per-audit plans, reports and graded findings
9.3Management review resultsMinutes recording decisions, owners and dates, not slides presented
10.2Nonconformities and corrective actionsA log covering what failed, the cause, the action, the owner and proof the fix held

Records are where certification is really won or lost. Documents show the auditor what you intended; records show whether it happened, and Stage 2 is built on sampling them.

What auditors weigh is time. A risk register edited continuously over twelve months reads very differently from a perfect one last touched three weeks before the audit.

A record created the week before the audit is a document pretending to be evidence.

The strongest records are the ones nobody had to write. Ticket trails, training-platform completions, scanner exports and access review outputs exist because the work went through a system. When the auditor asks for evidence, you produce it from that system on demand instead of assembling a folder.

Free Resource - ISO 27001

The ISO 27001 readiness checklist

Ninety-eight controls mapped to what an assessor actually asks for, in the order they ask it. Written by practitioners who took our ISMS through certification.

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Which Annex A controls usually need documents?

No Annex A control is mandatory, so no Annex A document is mandatory either. Once your Statement of Applicability marks a control as applicable, auditors usually expect written rules, procedures or records behind it. The most common are topic-specific policies, the asset inventory, access control rules, incident procedures, continuity plans and the legal register.

The table lists the documents we see requested most often when the control applies. Treat it as a checklist to test against your own Statement of Applicability, not a list to produce wholesale.

Annex A controlDocument usually expectedWhat makes it hold up
A.5.1 Policies for information securityTopic-specific policiesManagement approval, communication to the people they apply to, planned reviews
A.5.9 Inventory of information and other associated assetsAsset inventoryNamed owners, and a link to the risks each asset carries
A.5.10 Acceptable useAcceptable use rulesAcknowledged by staff and contractors
A.5.15 Access controlAccess control rulesMatched by what the identity provider actually enforces
A.5.24 Incident management planning and A.5.26 ResponseIncident management procedureRoles, escalation and a record of real or rehearsed use
A.5.30 ICT readiness for business continuityICT continuity plansRecovery targets and test results
A.5.31 Legal, statutory, regulatory and contractual requirementsRegister of obligationsKept current and cross-referenced to policies
A.5.37 Documented operating proceduresOperating proceduresAvailable to the people who run the systems
A.8.9 Configuration managementStandard configurationsEnforced as code or baseline, with drift detected
A.8.13 Information backupBackup rulesJob history and at least one test restore
A.8.15 LoggingLogs (records)Retained, protected and actually reviewed
A.8.24 Use of cryptographyRules for cryptographyApproved methods and key management named
A.8.32 Change managementChange procedureChange tickets showing assessment, approval and testing

Two rules keep this list under control.

  • Write only what the Statement of Applicability needs. If you have justified excluding a control, you do not need its document. If a control applies, its document must describe what you really do.
  • Document the rule, not the tool. "Production access requires multi-factor authentication and a manager's approval" survives a change of identity provider. A forty-step console walkthrough does not.

For how each of the 93 controls fits together, see the ISO 27001 Annex A controls guide.

How much ISO 27001 documentation is enough?

Clause 7.5 asks for the documented information the standard names, plus whatever you decide the ISMS needs to work effectively. The right extent depends on your size, activities and complexity, so a 60-person software firm needs far less than a bank. Enough means every process an auditor samples can be shown working from what you hold.

Over-documentation is the more common failure at this size. Template packs arrive with dozens of policies and procedures written for organisations with departments you don't have. Each one becomes a promise.

A 40-page policy nobody has read isn't evidence of control.

The risk is specific. An auditor who samples a procedure will test whether you follow it. If the document says access reviews happen monthly and your records show two a year, that gap is a nonconformity against your own rules, even though the standard never asked for monthly reviews.

Three tests decide whether a document earns its place:

  1. Does the standard or an applicable control require it? If yes, it stays.
  2. Would a new joiner do the task wrongly without it? If yes, it stays, written as briefly as the task allows.
  3. Does it describe what actually happens? If not, fix the document or fix the practice before the auditor finds the difference.

Applied honestly, those tests usually leave a compact set. For a 60-person software firm with whole-organisation scope, a credible set looks like this:

  • the clause-required documents from the first table, each a few pages at most;
  • one information security handbook carrying the topic-specific policies, a section per topic;
  • a handful of procedures for the tasks that go wrong without them: incident response, access changes, joiners and leavers, change and release, backup and restore;
  • the asset inventory, the obligations register and the risk register as living registers, not documents.

Everything else is a record the systems already produce.

How you control these documents is a separate question: identifiers, versioning, approval, access, retention and disposal. The Clause 7.5 documented information guide covers that in depth.

How do you keep ISO 27001 documents audit-ready?

Give every document a named owner, a version and a review date, keep them in a single register, and let the systems that do the work generate your records. The auditor's request list then becomes a set of links, and the documents stay accurate between audits instead of being refreshed the month before.

A working set-up at this scale has four parts:

  • One register. A spreadsheet or database view listing each document, its owner, version, status and next review date is enough. Nobody expects a document-management suite at 50 people.
  • Named owners. Each document has one person accountable for keeping it true, and an approver who is not its author.
  • Review triggers as well as dates. An annual review is a minimum, not a method. A new cloud provider, an incident or a restructure should open a review of the documents it touches.
  • Generated evidence. Connect the register to the systems that hold proof: the identity provider for access reviews, the ticketing tool for changes, the training platform for awareness.

That last step is where GRC Engineering pays off. When evidence is collected continuously from the systems that do the work, audit preparation shrinks from weeks of chasing to a check that the feeds are still running.

The same set answers more than the auditor. Enterprise security questionnaires ask for your policy, your scope, your incident procedure and proof of review. A document set that is current, owned and evidenced turns those questionnaires from a scramble into a reply.

If you are starting from an inherited folder, an ISO 27001 gap analysis will show which of these documents exist and which only look as if they do. The ISO 27001 implementation roadmap sets out when each one gets written, and the certification process guide shows where each one is tested.

Frequently asked questions

Yes, provided you rewrite them to describe your organisation. Auditors spot template language quickly: roles you don't employ, committees that never meet, review cycles nobody runs. Use a template for structure and headings, then delete anything you can't evidence. A short document that matches reality beats a long one that doesn't.

Yes. The standard leaves format and medium to you. What matters is that each document has an identity, a version history, a recorded approval and controlled edit rights. A wiki with page history and restricted editing often meets this better than shared drives full of files named "final v3".

At planned intervals you define, and whenever a significant change makes them inaccurate. Annual review is the common baseline. Record each review even when nothing changes, with the date and the reviewer, because "reviewed, no change needed" is evidence and silence is not.

No. One document, or one system record, can address several controls. Add a reference column to the Statement of Applicability that points each applicable control to the document section or system that addresses it. The auditor can then follow the trail from control to evidence without asking you to find it.

The standard leaves retention periods to you, so set them in a retention schedule and apply them consistently. As a working minimum, keep ISMS records for at least one full three-year certification cycle, so the recertification auditor can see the whole period. Legal and contractual obligations, such as employment or financial record rules, may require longer.

The Stage 1 auditor will record it as a gap to close before Stage 2. Depending on how much is missing, the certification body may delay Stage 2 until it is fixed. Closing the gap takes longer than writing the document, because it also needs approval, communication and enough operating time to produce records.

Profile image for Harry West, Founder and CEO of GRCMANA
Author

Harry West

Harry is the founder of GRCMANA, he helps regulated service providers close the enterprise trust gap — turning GRC, cyber resilience and AI governance from paperwork exercises into shippable systems.

Standard engine

ISO 27001 reference directory.

Every control in this framework and the clause guides that sit above them, grouped by control domain. Open any entry for its control definition, implementation steps and the audit evidence it expects. Dimmed entries are planned.

ClausesThe management systemClause guides · 23 guides
Clause 4.1Understanding the organization and its context→Clause 4.2Understanding the needs and expectations of interested parties→Clause 4.3Determining the scope of the information security management system→Clause 4.4Information security management system→Clause 5.1Leadership and commitment→Clause 5.2Policy→Clause 5.3Organizational roles, responsibilities and authorities→Clause 6.1Actions to address risks and opportunities→Clause 6.2Information security objectives and planning to achieve them→Clause 7.1Resources→Clause 7.2Competence→Clause 7.3Awareness→Clause 7.4Communication→Clause 7.5Documented information→Clause 8.1Operational planning and control→Clause 8.2Information security risk assessment→Clause 8.3Information security risk treatment→Clause 9.1Monitoring, measurement, analysis and evaluation→Clause 9.2Internal audit→Clause 9.2Preparing for Your ISO 27001 Stage 2 Audit: A Practical Checklist→Clause 9.3Management review→Clause 10.1Continual improvement→Clause 10.2Nonconformity and corrective action→
A.5Organizational Controls37 guides
A.5.1Policies for information security→A.5.2Information security roles and responsibilities→A.5.3Segregation of duties→A.5.4Management responsibilities→A.5.5Contact with authorities→A.5.6Contact with special interest groups→A.5.7Threat intelligence→A.5.8Information security in project management→A.5.9Inventory of information and other associated assets→A.5.10Acceptable use of information and other associated assets→A.5.11Return of assets→A.5.12Classification of information→A.5.13Labelling of information→A.5.14Information transfer→A.5.15Access control→A.5.16Identity management→A.5.17Authentication information→A.5.18Access rights→A.5.19Information security in supplier relationships→A.5.20Addressing information security within supplier agreements→A.5.21Managing information security in the ICT supply chain→A.5.22Monitoring, review and change management of supplier services→A.5.23Information security for use of cloud services→A.5.24Information security incident management planning and preparation→A.5.25Assessment and decision on information security events→A.5.26Response to information security incidents→A.5.27Learning from information security incidents→A.5.28Collection of evidence→A.5.29Information security during disruption→A.5.30ICT readiness for business continuity→A.5.31Legal, statutory, regulatory and contractual requirements→A.5.32Intellectual property rights→A.5.33Protection of records→A.5.34Privacy and protection of PII→A.5.35Independent review of information security→A.5.36Compliance with policies, rules and standards for information security→A.5.37Documented operating procedures→
A.6People Controls8 guides
A.6.1Screening→A.6.2Terms and conditions of employment→A.6.3Information security awareness, education and training→A.6.4Disciplinary process→A.6.5Responsibilities after termination or change of employment→A.6.6Confidentiality or non-disclosure agreements→A.6.7Remote working→A.6.8Information security event reporting→
A.7Physical Controls14 guides
A.7.1Physical security perimeters→A.7.2Physical entry→A.7.3Securing offices, rooms and facilities→A.7.4Physical security monitoring→A.7.5Protecting against physical and environmental threats→A.7.6Working in secure areas→A.7.7Clear desk and clear screen→A.7.8Equipment siting and protection→A.7.9Security of assets off-premises→A.7.10Storage media→A.7.11Supporting utilities→A.7.12Cabling security→A.7.13Equipment maintenance→A.7.14Secure disposal or re-use of equipment→
A.8Technological Controls34 guides
A.8.1User endpoint devices→A.8.2Privileged access rights→A.8.3Information access restriction→A.8.4Access to source code→A.8.5Secure authentication→A.8.6Capacity management→A.8.7Protection against malware→A.8.8Management of technical vulnerabilities→A.8.9Configuration management→A.8.10Information deletion→A.8.11Data masking→A.8.12Data leakage prevention→A.8.13Information backup→A.8.14Redundancy of information processing facilities→A.8.15Logging→A.8.16Monitoring activities→A.8.17Clock synchronization→A.8.18Use of privileged utility programs→A.8.19Installation of software on operational systems→A.8.20Networks security→A.8.21Security of network services→A.8.22Segregation of networks→A.8.23Web filtering→A.8.24Use of cryptography→A.8.25Secure development life cycle→A.8.26Application security requirements→A.8.27Secure system architecture and engineering principles→A.8.28Secure coding→A.8.29Security testing in development and acceptance→A.8.30Outsourced development→A.8.31Separation of development, test and production environments→A.8.32Change management→A.8.33Test information→A.8.34Protection of information systems during audit testing→
OtherAdditional Guides7 guides
GuideISO 27001 Statement of Applicability: what it is, with a worked example→GuideISO 27001 implementation→GuideISO 27001 certification and audit process→GuideISO 27001 mandatory documents and records→GuideISO 27001 gap analysis→GuideISO 27001 certification cost→GuideISO 27001 Annex A controls→
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