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AI Management Systems Β· ISO/IEC 42001:2023

ISO/IEC 42001:2023 Documentation Toolkit

The real ISO/IEC 42001:2023 documentation set we deliver: 138 documents and six validated Excel tools that form a complete AI management system (AIMS) for an organisation that deploys AI. Every requirement in clauses 4 to 10 is owned by a procedure or the manual, and all 38 Annex A controls are mapped in the Statement of Applicability. You get the AIMS Manual, AI Policy, 19 procedures, 6 work instructions, 51 forms each with a completed worked example, and the risk, impact, Statement of Applicability and KPI tools, all editable in Word and Excel, so you can build a certification-ready AI governance system without hiring a consultant.

138
Documents
and tools
19
Procedures
clause-mapped
51
Forms with
filled samples
6
Validated
Excel tools
$149
βœ“ Within 24h secure deliveryβœ“ Editable Word and Excelβœ“ Lifetime free updates
ISO/IEC 42001:2023MANUAL
AI Management Systems System Manual
Clause-by-clause structure
19Clause-mapped
procedures
51Ready-to-use
forms
Written to satisfy the requirements checked byBSISGSTÜVBureau VeritasDNVIntertek
Overview

Everything you need for ISO/IEC 42001:2023, in one download

Preparing the documentation is the slowest and most confusing part of getting certified to ISO/IEC 42001:2023. You have to work out what the standard asks for, decide what to write, and turn it into a manual, procedures and records that an auditor will accept. Done from a blank page it takes months, and paying a consultant to do it can cost thousands.

The ISO/IEC 42001:2023 Documentation Toolkit gives you that whole system, already written and ready to edit. It is built by practitioners around the exact structure of the standard, so nothing an auditor expects is missing. You add your company details, adapt anything specific to your operation, and you have a complete, consistent ai management systems system that is ready for audit. Every single document you receive is listed and explained further down this page, so you know precisely what you are buying before you spend anything.

What makes this set specific

Built for your real production model, not a generic template

Built for organisations that deploy AI

The system is written for a deployer of AI, the most common role, not a model developer. It covers selecting, configuring, validating, deploying, monitoring and decommissioning third-party AI systems, and it is threaded through a realistic healthcare example you replace with your own.

Every clause and all 38 Annex A controls covered

Every requirement in clauses 4 to 10 (32 subclauses) is owned by a procedure or the manual, and all 38 Annex A controls are listed and justified in the Statement of Applicability, so nothing an auditor checks is missing.

AI risk and AI system impact assessment

Dedicated procedures, work instructions and Excel tools for AI risk assessment and treatment, and for the AI system impact assessment on individuals and society that ISO 42001 requires beyond a conventional risk register.

A completed example for every form

All 51 forms come with a matching sample filled form, completed around the example organisation, so you can see exactly how each record should look before you fill your own.

Six validated Excel tools

Working tools, not blank sheets, for the AI risk register, the Statement of Applicability, impact-assessment scoring, the competence matrix and gap analysis, the AIMS KPI dashboard, and the internal audit and nonconformity tracker.

Guided tailoring before certification

Three customization guides walk you through replacing placeholders, making the configuration decisions the toolkit leaves to you, and reviewing every document against your real operations before you seek certification.

How the set is structured

138 controlled documents in 8 tiers

Each tier answers a different question and is approved at a different level, and every requirement is owned in exactly one place.

MAN1AI Management System Manual
POL1AI Policy
QP19Procedures
WI6Work instructions
QF51Forms and registers
SMP51Sample filled forms
TOOL6Validated Excel tools
CUST3Customization guides
The full contents

Every document in this toolkit, listed and explained

No hidden contents and no vague claims. Here is the complete document set, with a short description of what each file is for and the clause it helps you meet.

ISO/IEC 42001:2023 Toolkit

A complete document set, fully editable in Microsoft Office.

AI Management System Manual1
AI Policy1
Procedures19
Work instructions6
Forms and registers51
Sample filled forms51
Validated Excel tools6
Customization guides3
Total documents138

MAN-01 AI Management System Manual

The controlling document of the AIMS. It demonstrates, clause by clause, how the organisation meets ISO/IEC 42001:2023 and traces each requirement to the procedures, forms, tools and records that satisfy it. Sections 4 to 10 follow the clause structure exactly, and Annexes A to G carry the process map, clause cross-reference matrix, Statement of Applicability summary and KPIs. This is the document an auditor opens first.

Introduction and organisation overviewScope, normative references and terms4. Context of the organisation5. Leadership and AI policy6. Planning: AI risk, impact and objectives7. Support8. Operation across the AI life cycle9. Performance evaluation10. ImprovementAnnexes A to G: process map, clause matrix, Statement of Applicability, KPIs
POL AI Policy (1)
  • POL-01 AI Policy. Top management commitment to responsible AI: the principles, objectives and boundaries that govern how the organisation develops or deploys AI, aligned to ISO/IEC 42001 Clause 5.2.
QP Procedures (19)
  • QP-01 Control of Documented Information. How AIMS documents and records are created, approved, issued, changed and controlled.
  • QP-02 Context, Interested Parties and AIMS Scope. How the organisation determines its context, its interested parties and their needs, and sets the scope of the AIMS (Clause 4).
  • QP-03 Leadership, Roles, Responsibilities and Concern Reporting. How leadership is exercised, roles and authorities are assigned, and staff can raise AI concerns (Clause 5).
  • QP-04 AI Risk Management. How AI-related risks are identified, analysed, evaluated and treated against defined criteria (Clause 6.1).
  • QP-05 AI System Impact Assessment. How the impact of an AI system on individuals, groups and society is assessed, which ISO 42001 requires beyond ordinary risk.
  • QP-06 AI Objectives and Planning of Changes. How AI objectives are set and monitored and how changes to the AIMS are planned and controlled (Clause 6.2 and 6.3).
  • QP-07 Competence, Awareness and Communication. How competence is built, awareness is maintained and internal and external communication is managed (Clause 7).
  • QP-08 Operational Planning and Control. How the operational controls of the AIMS are planned and executed across the AI life cycle (Clause 8.1).
  • QP-09 AI System Life Cycle Management. How AI systems are specified, selected, validated, deployed and decommissioned through their life cycle.
  • QP-10 Data Management for AI Systems. How data used by AI systems is sourced, documented, quality-checked and its provenance recorded.
  • QP-11 AI Resources and System Inventory. How AI systems and their supporting resources are inventoried and documented.
  • QP-12 Information for Interested Parties and Incident Communication. How information is provided to users and affected parties and how AI incidents are communicated.
  • QP-13 Responsible Use of AI Systems. How intended and acceptable use is defined and responsible-use objectives are set and monitored.
  • QP-14 Third-Party, Supplier and Customer Relationships. How AI suppliers and customers are evaluated, approved and managed, and responsibilities allocated.
  • QP-15 Monitoring, Measurement, Analysis and Evaluation. How AIMS performance and the AI systems are monitored and evaluated against objectives and KPIs (Clause 9.1).
  • QP-16 Internal Audit. How internal audits of the AIMS are planned, conducted and reported (Clause 9.2).
  • QP-17 Management Review. How top management reviews the AIMS and sets actions (Clause 9.3).
  • QP-18 Nonconformity, Corrective Action and Continual Improvement. How nonconformities are handled, corrective action is taken and improvement is driven (Clause 10).
  • QP-19 AIMS Maintenance and Standard Revision. How the AIMS is maintained over time and updated when ISO/IEC 42001 or related standards are revised.
WI Work instructions (6)
  • WI-04-01 Performing an AI Risk Assessment. Step-by-step method for running an AI risk assessment and recording it, using the risk register tool.
  • WI-05-01 Performing an AI System Impact Assessment. Step-by-step method for assessing an AI system impact on people and society, using the scoring tool.
  • WI-09-01 AI System Pre-Deployment Validation and Acceptance. How to validate and formally accept an AI system before it goes live.
  • WI-09-02 AI System Monitoring and Event Logging. How to monitor a live AI system and keep the event log that evidences oversight.
  • WI-10-01 Data Quality Evaluation for AI. How to evaluate the quality of the data used by an AI system.
  • WI-16-01 Conducting an Internal AIMS Audit. How to plan, run and report an internal audit of the AI management system.
QF Forms and registers (51)
  • QF-01-01 Master Document Register. The master index of every controlled AIMS document.
  • QF-01-02 Document Change Request. Requests and records a change to a controlled document.
  • QF-01-03 Controlled Distribution List. Records who holds controlled copies of documents.
  • QF-02-01 Context and Issues Register. Records the internal and external issues that shape the AIMS.
  • QF-02-02 Interested Parties and Requirements Register. Records interested parties and their relevant requirements.
  • QF-02-03 AIMS Scope Statement. States the boundaries and applicability of the AIMS.
  • QF-03-01 AI Roles and Authorities (RACI) Matrix. Assigns AI responsibilities and authorities across roles.
  • QF-03-02 AI Concern Reporting Form. Lets staff raise a concern about an AI system or its use.
  • QF-04-01 AI Risk Criteria Register. Defines the criteria used to evaluate AI risk.
  • QF-04-02 AI Risk Assessment Register. Records identified AI risks, their analysis, score and band.
  • QF-04-03 AI Risk Treatment Plan. Plans and tracks the treatment of AI risks.
  • QF-04-04 Statement of Applicability Record. Records which Annex A controls apply and why.
  • QF-05-01 AI System Impact Assessment Form. Captures the impact assessment for an AI system.
  • QF-06-01 AI Objectives and Action Plan. Sets AI objectives and the actions to achieve them.
  • QF-06-02 Change Request and Plan. Plans a change to the AIMS or an AI system.
  • QF-07-01 AI Competence Matrix. Maps roles against the AI competencies they need.
  • QF-07-02 Training Needs Analysis and Plan. Identifies training needs and plans the training.
  • QF-07-03 Training Attendance and Effectiveness Record. Records training delivered and its effectiveness.
  • QF-07-04 Awareness Briefing Record. Records AI awareness briefings to staff.
  • QF-07-05 Communication Plan. Plans internal and external AIMS communication.
  • QF-08-01 Operational Control Plan. Defines the operational controls applied across the AI life cycle.
  • QF-09-01 AI System Requirements Specification. Specifies what an AI system must do before selection.
  • QF-09-02 AI System Selection and Evaluation Record. Records the selection and evaluation of an AI system.
  • QF-09-03 AI System Verification and Validation Record. Records verification and validation of an AI system.
  • QF-09-04 AI System Deployment Plan and Approval. Plans and approves the deployment of an AI system.
  • QF-09-05 AI System Technical Documentation Index. Indexes the technical documentation for an AI system.
  • QF-09-06 AI System Event Log Register. Logs events and oversight actions for a live AI system.
  • QF-10-01 Data Resource Register. Registers the data resources used by AI systems.
  • QF-10-02 Data Provenance Record. Records the origin and lineage of AI data.
  • QF-10-03 Data Quality Assessment. Assesses the quality of data used by an AI system.
  • QF-11-01 AI System Inventory and Asset Register. Inventories the AI systems and related assets in scope.
  • QF-11-02 Resource Documentation Record. Documents the resources supporting an AI system.
  • QF-12-01 AI System Information Sheet (System Card). A system card describing an AI system, its intended use and the human oversight applied.
  • QF-12-02 External Adverse-Impact Reporting Log. Logs externally reported adverse impacts of AI.
  • QF-12-03 Incident Communication Record. Records communication about an AI incident.
  • QF-13-01 AI Acceptable and Intended-Use Register. Records the intended and acceptable uses of each AI system.
  • QF-13-02 Responsible Use Objectives Record. Records responsible-use objectives and their monitoring.
  • QF-14-01 Supplier Evaluation and Approval. Evaluates and approves an AI supplier.
  • QF-14-02 Responsibility Allocation Matrix (Third Party). Allocates responsibilities between the organisation and third parties.
  • QF-14-03 Approved AI Supplier Register. The register of approved AI suppliers.
  • QF-15-01 AIMS KPI and Monitoring Plan. Defines the KPIs and the monitoring plan for the AIMS.
  • QF-16-01 Annual Internal Audit Programme. Plans the internal audit programme for the year.
  • QF-16-02 Individual Audit Plan. Plans a single internal audit.
  • QF-16-03 AIMS Audit Checklist. The checklist used to audit the AIMS against the standard.
  • QF-16-04 Internal Audit Report. Reports the findings of an internal audit.
  • QF-16-05 Nonconformity Report. Records a nonconformity found in the AIMS.
  • QF-17-01 Management Review Agenda. The agenda for a management review.
  • QF-17-02 Management Review Input Pack. The inputs assembled for a management review.
  • QF-17-03 Management Review Minutes and Action Log. Records the management review decisions and actions.
  • QF-18-01 Corrective Action Request (CAPA). Raises and tracks a corrective action.
  • QF-18-02 Continual Improvement Log. Logs continual improvement actions.
Every form above is also provided as a completed sample filled form, worked around the example organisation, so you can see exactly how each record should look. That is 51 additional worked examples included in the set.
TOOL Validated Excel tools (6)
  • T-01 AI Risk Assessment and Treatment Register. Working register that scores AI risks and tracks their treatment.
  • T-02 Statement of Applicability. Maps all 38 Annex A controls with applicability and justification.
  • T-03 AI System Impact Assessment Scoring Tool. Scores the impact of an AI system on individuals and society.
  • T-04 AI Competence Matrix and Gap Analysis. Scores competence against roles and highlights the gaps.
  • T-05 AIMS KPI Dashboard. Tracks the AIMS KPIs and shows performance at a glance.
  • T-06 Internal Audit and Nonconformity Tracker. Tracks audits, findings and nonconformities to closure.
CUST Customization guides (3)
  • CUST-01 Customization Guide. How to tailor the whole toolkit to your organisation before certification.
  • CUST-02 Placeholder Replacement Guide. The list of placeholders to replace, so no example content is left behind.
  • CUST-03 Configuration Decision Checklist. The configuration decisions the toolkit leaves to you, gathered in one checklist.
What you gain

Why teams choose a ready-made kit

βœ“
Save months of work

The writing is done. You edit instead of authoring from a blank page.

βœ“
Avoid consultant fees

Get a professional system for a fraction of the cost of hiring one.

βœ“
Nothing missed

Mapped clause by clause so every requirement is covered.

βœ“
Written in plain English

Easy to read, easy to adapt, no jargon you have to decode.

βœ“
Audit-ready evidence

Forms and registers capture exactly what an auditor asks to see.

βœ“
Yours to keep

A perpetual licence for your whole team, with free updates.

How to use it

From download to audit ready in five steps

Download

The full set arrives by email in minutes, in Word and Excel.

Customise

Swap the highlighted placeholders for your own company details.

Implement

Roll out the procedures and capture evidence on the forms.

Audit and review

Use the internal audit checklist and management review templates.

Get certified

Face the auditor with a complete, consistent system.

Who it is for

Built for the people who have to get it done

  • Companies going for ISO/IEC 42001:2023 certification for the first time.
  • Quality and compliance managers who want a proven framework, not a blank page.
  • Businesses asked for a documented system for a tender, a client, or pre-qualification.
  • Consultants and trainers who need an editable base to adapt for clients.
How it is delivered

Secure, editable, and yours to keep

πŸ“₯

24-hour delivery

Files sent securely within 24 working hours of payment.

✍️

Fully editable

Microsoft Word and Excel, with placeholders to fill in.

♾️

Free updates

If the standard is revised, you get the update free.

πŸ‘₯

Team licence

One organisation, unlimited internal users, perpetual.

Compare the options

Kit, consultant, or from scratch

What mattersFrom scratchHire a consultantisofolder kit
Time to a full document setMonthsWeeksThe same day
Typical costYour timeThousands$149 once
Written by expertsNoYesYes
Mapped to every clauseRiskyUsuallyYes
You keep full controlYesLimitedYes, fully editable
Free updates on revisionNoExtra feeIncluded
Our experience

Documentation is all we do, and we have done it since 2017

isofolder is a team of auditing and consulting professionals with more than 80 years of combined experience. Our kits are written by practitioners and reviewed by working auditors, then refined across many real certification projects. When you buy from us, you are buying a system that has already helped companies pass their audits.

If you ever need a document that is specific to your operation and not already in the kit, our team will prepare it for you.

2017Trading since
2,000+Products delivered
750+Projects completed
100+Standards covered
What buyers say

Trusted by teams getting certified

β˜…β˜…β˜…β˜…β˜…

The documents were well structured and easy to adapt. We cleared our certification audit with no major findings.

Quality ManagerManufacturing, United Kingdom
β˜…β˜…β˜…β˜…β˜…

Saved us weeks of writing. Everything was mapped to the clauses, so we knew nothing was missing.

Operations LeadFood business, UAE
β˜…β˜…β˜…β˜…β˜…

Clear, professional and fully editable. Far better value than the consultant quotes we received.

FounderServices company, United States
See it first

Not sure yet? Look inside before you buy

Preview 11 real pages from the ISO/IEC 42001:2023 toolkit right here, including a full form and part of an actual procedure. Judge the quality and writing style for yourself, with no sign-up.

Questions

ISO/IEC 42001:2023 toolkit, frequently asked

What is ISO/IEC 42001 and who needs it?+
ISO/IEC 42001:2023 is the world's first management system standard for artificial intelligence. It sets out how an organisation governs the AI systems it develops or deploys, covering AI policy, risk, the AI system impact assessment, human oversight, data and supplier management. Any organisation that builds or uses AI and wants to show responsible, auditable AI governance can certify to it.
Does this toolkit cover all 38 Annex A controls?+
Yes. Every requirement in clauses 4 to 10 of ISO/IEC 42001:2023 is owned by a procedure or the manual, and all 38 Annex A controls are listed and justified in the Statement of Applicability tool and implemented through the procedures.
Is it for AI developers or AI users?+
It is written for an organisation that deploys AI, which is the most common role, and it is threaded through a realistic healthcare deployer example. The controls concerned with model development and training-data creation apply in the narrower sense of configuration, evaluation data, validation and monitoring, and the Statement of Applicability records the justification. A developer can adopt it and widen those controls.
What are the AI risk and impact assessment parts?+
ISO 42001 requires both an AI risk assessment and an AI system impact assessment, which considers effects on individuals and society, not only on the organisation. The toolkit includes dedicated procedures, work instructions and Excel tools for both, with worked examples.
Does every form come with a filled example?+
Yes. All 51 forms are provided both blank and as a completed sample filled form, worked around the example organisation, so you can see exactly how each record is meant to look before completing your own.
What does the ISO/IEC 42001:2023 toolkit include?+
A clause-by-clause ISO/IEC 42001:2023 manual, 19 procedures, and 51 ready-to-use forms and records, plus sample filled examples. Everything is editable in Microsoft Word and Excel, and the full list is shown on this page.
Will it help me pass a certification audit?+
Yes. The documents are structured to the ISO/IEC 42001:2023 clauses an auditor checks and are written by experienced practitioners. You customise and implement them, and the kit gives you a complete, auditor ready system as your foundation.
What formats do I get, and can I edit them?+
Everything comes in editable Microsoft Word and Excel, with any presentations in PowerPoint. You replace the highlighted placeholders with your own details. No special software is needed.
How long does it take to customise?+
Most organisations tailor the core documents within a few days rather than the weeks or months it takes to write from a blank page. The manual and procedures are already written, so you are editing, not authoring.
How is it delivered?+
After your payment is confirmed, we send your files to you securely within 24 working hours, and usually much sooner. To keep the documents safe, we do not store them on public-facing servers.
Is there a licence limit or a subscription?+
There is no subscription. One purchase gives your organisation a perpetual licence with unlimited internal users, so your whole team can work on the documents.
Do I get updates when the standard changes?+
If ISO/IEC 42001:2023 is revised, you receive the updated documents free of charge, so your system stays current without buying again.
Is it suitable for my industry?+
The kit is written to the ISO/IEC 42001:2023 requirements, which apply across sectors. The documents are editable, so you keep what fits your operation and adapt or set aside anything that does not. It has been used by manufacturers, food businesses, laboratories, healthcare, IT and service companies.
How is this different from free templates online?+
Free templates are usually incomplete, generic, or out of date, and they leave you guessing what an auditor expects. This kit is a complete, current, clause-mapped set written by practitioners, with every document listed and explained so there are no surprises.
Can I check the toolkit before I buy?+
Yes. You can download a free sample document first to check the quality and writing style, so you can decide with confidence.
Complete your system

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ISO/IEC 42001:2023 Documentation Toolkit 138 documents, Word and Excel, delivery within 24 working hours $149