ISO/IEC 42001 guide
ISO 42001 implementation plan: the phases, owners, deliverables and decision points of an ISO/IEC 42001 project
Clause by clause: ISO/IEC 42001:2023 requirements: every clause explained →
How to run ISO/IEC 42001 as a project: seven phases over four to eight months, each with weeks, deliverables, an owner and a management decision, the roles that carry the work, and how Design™ or Drive™ changes who does it.
Key points
- An ISO/IEC 42001 implementation plan turns the AIMS into a project: every piece of work has an owner, a deliverable, a week range and the management decision it waits for.
- Seven overlapping phases usually take an organisation from kick-off to the certification decision in four to eight months; an existing ISO/IEC 27001 system puts you at the shorter end.
- The plan starts with an inventory of AI systems, because the risk assessments, impact assessments and Statement of Applicability are all built per system.
- Design™ and Drive™ are alternative routes: they change who drafts and who chases actions, never who approves the treatment plan or who answers the auditor.
What an ISO/IEC 42001 implementation plan covers
ISO/IEC 42001 does not require a project plan; it requires an AI management system that operates. The plan is how you get there without losing months: a one-page schedule naming, for each block of work, its owner, its output, its weeks and the decision it waits for.
Three things set an AIMS project apart. The unit of work is the AI system: each one in scope needs an owner, a risk assessment, an impact assessment and life-cycle records, so the inventory sets the size of the plan. The Planning clause gives management a formal decision, approving the AI risk treatment plan and accepting the residual risks, which belongs in the schedule as a dated gate. And AI systems change while you implement, so the plan needs a trigger for reassessment after significant change.
The phases: weeks, deliverables, owners and decision points
Ranges assume a manageable number of AI systems in scope; your plan puts a date on each row.
| Phase | Weeks | Deliverables | Owner | Decision point |
|---|---|---|---|---|
| 1. Mobilise and inventory | 1 to 3 | An inventory of AI systems developed, provided or used, with your role for each; a draft scope; target date; named roles | Sponsor, with the AIMS lead | Sponsor approves the scope, the target date and people's time |
| 2. Gap analysis and action plan | 2 to 5 | A gap report against clauses 4 to 10 and Annex A; prioritised actions with owners and dates | Sterling consultant, with the AIMS lead | Sponsor accepts the action plan and the target audit window |
| 3. Policy, risk and impact | 4 to 14 | The AI policy and objectives; risk criteria and method; a risk assessment and an impact assessment per system; the Statement of Applicability; the risk treatment plan | AIMS lead and AI system owners | Designated management approves the treatment plan and accepts the residual risk |
| 4. Operate the controls, train, contract | 6 to 26 | Life-cycle, data and supplier records; event logs; awareness and role training; internal auditors trained; accredited certification body contracted | AI system owners and AIMS lead | Sponsor appoints the certification body and fixes Stage 1 and Stage 2 dates |
| 5. Internal audit and management review | 14 to 28 | Audit of clauses and applicable controls; corrective actions closed; the management review record | Internal auditors; top management | Management review decides: ready for Stage 1, or not yet |
| 6. Certification audits | 18 to 35 | Stage 1 readiness review and any concerns closed; Stage 2; responses to findings | AIMS lead; the audits are the certification body's | The certification body takes the certification decision |
| 7. Sustain™ | From the decision | Year-one calendar of reassessments, audits and reviews | AIMS lead and AI system owners | Sponsor confirms the year-one calendar |
Phases 3 and 4 overlap on purpose. Once one system's treatment is agreed, its controls start producing records while the next is still being assessed. The detailed calendar and the certification body's lead times sit in ISO/IEC 42001 timeline: how long certification takes, stage by stage; what the phase 2 report contains is covered in ISO/IEC 42001 gap analysis: what it covers and what you get.
Who does the work: the roles in an AIMS project
The Leadership clause makes top management responsible for the AIMS and requires roles, responsibilities and authorities to be assigned; Annex A adds a control on AI roles and responsibilities. In project terms that gives five roles.
- Sponsor. A member of top management who owns the target date, releases people's time and takes the decisions in the table. Accepting residual AI risk is a management judgement, not a technical sign-off, so this is where the sponsor's attention matters most.
- AIMS lead. Runs the weekly session, keeps the inventory and documented information in order and prepares the audits.
- AI system owners. One accountable person per system in scope, who takes part in its assessments, keeps its life-cycle and data records current and explains it at Stage 2.
- Contributors. Data scientists and engineers for design, verification and data provenance; legal and privacy for obligations; procurement for suppliers of models and data. Budget their hours, because they are rarely free.
- Internal auditors. At least two trained people who can audit areas other than their own and understand AI life-cycle practice well enough to test the records. ISO/IEC 42001 internal audit: auditing an AI management system covers the method.
Design™ or Drive™: choosing the route
In Sterling OS™, the method behind every Sterling engagement, Design™ and Drive™ are alternative routes through phases 1 to 6; you take one or the other. Under Design™ your team implements while Sterling coaches and runs workshops; under Drive™ Sterling's consultants carry the agreed share of the work with your system owners. Automate™, the AIMS in Effivity, spans every phase, and Sustain™ is phase 7.
| Work in the plan | Design™ (guided) | Drive™ (managed) |
|---|---|---|
| AI system inventory and gap analysis | Sterling, with your AIMS lead and system owners | The same |
| AI policy, risk method, Statement of Applicability | Drafted by your team in workshops on Sterling's structure; Sterling reviews | Drafted by Sterling consultants; your AIMS lead corrects and adopts |
| Risk and impact assessments per system | Run by your system owners with Sterling facilitating the first ones | Facilitated by Sterling for each system, with the owner and contributors in the room |
| Actions between weekly sessions | Your AIMS lead and system owners | Mainly Sterling consultants |
| Life-cycle, data and supplier records | Your people, as part of their work | The same |
| Treatment plan approval and management review | Your top management | The same |
Design™ suits an AIMS lead with time and owners used to documenting their work, often where an ISMS already runs. Drive™ suits a fixed customer or tender deadline, many AI systems or technical teams with no drafting time. Neither route shortens how long the controls must operate before Stage 2.
Five mistakes that stall ISO/IEC 42001 projects
- Starting without an inventory. Teams write the AI policy first, then find systems nobody listed, including AI features inside tools already bought.
- Treating the impact assessment as a report. Written once, filed and forgotten, it never feeds the risk assessment as the standard requires. Schedule it inside phase 3 for each system and link its results to the risk register.
- Leaving third-party models out of the plan. A supplier's model brings responsibilities, documentation requests and checks that need owners and dates.
- Building a second system beside the ISMS. Separate document control, audits and reviews double the effort. Extend what exists; ISO/IEC 27001 to ISO/IEC 42001: extending an ISMS into an AIMS shows how.
- Contracting the certification body late. Accredited ISO/IEC 42001 certification is newer than for established standards, and auditor availability can set your Stage 1 date. Choose the body in phase 4, not after the management review.
Keeping the plan and the evidence in one place
A plan in a spreadsheet and evidence in shared drives drift apart. In a Sterling engagement both sit in Effivity, the Sterling group's ISO and GRC platform, used in 50+ countries and included with the engagement at no additional cost: actions and milestones with owners and due dates, the AI system inventory as a register configured for you, the risk register and treatment plan, and the audit, corrective action and review records. More detail is in Effivity for ISO/IEC 42001: the guide.
How Sterling runs your AIMS project
A dated plan, an owner for every AI system, and a decision at every gate.
Our gap analysis ends in your implementation plan, worked back from the date your customer, tender or board needs. You choose Design™ or Drive™, and Effivity carries the plan and the records from the first workshop. Ask a Sterling consultant for a phased plan built around your AI systems, sites and deadline; it is yours to keep, at no charge. We ensure successful certification for our clients. An independent, accredited certification body takes the certification decision; Sterling does not certify.
Book a free discovery callISO/IEC 42001 implementation plan: questions buyers ask
What goes into an ISO 42001 implementation plan?
An ISO/IEC 42001 implementation plan lists the phases from scoping to certification with a week range, deliverables, an owner and a decision point for each. It starts from the AI system inventory, includes the approval of the risk treatment plan as a management gate, and ends with the year-one calendar that keeps the system running.
Who should lead an ISO/IEC 42001 project?
A person who knows how your AI systems are built or used and has the authority to chase technical, legal and procurement teams should lead it. Where an ISMS exists, that is often the information security lead. Agree their project time in writing before kick-off.
Can our ISO/IEC 42001 project run inside our ISO/IEC 27001 programme?
Yes, and it usually should. Document control, internal audit, management review and corrective action can be shared, so the plan adds only the AI-specific work.
What if a new AI system goes live during the project?
Add it to the inventory, decide at the next weekly session whether it enters the scope now or later, and if it does, give it its own risk and impact assessment and records before Stage 2. If it would push the audit back too far, certify the agreed scope first and extend it at a later audit.
Is the implementation plan the same as the gap analysis?
No, the gap analysis produces the plan. The gap report shows what is missing against the standard; the plan turns that into phases, owners, dates and decisions. Both come after the free online readiness check and well before the certification body's Stage 1 readiness review.
More ISO/IEC 42001 guides
Every guide in the ISO/IEC 42001 series is written for one question and links back to the hub for the whole picture.
- AI system impact assessment, with ISO/IEC 42005
- ISO/IEC 42001 Annex A: the 38 controls explained
- ISO/IEC 42001 certification process, step by step
- ISO/IEC 42001 certification cost: what moves the price
- ISO/IEC 27001 to ISO/IEC 42001: extending an ISMS into an AIMS
- ISO 42001 gap analysis
- ISO 42001 for healthcare
- ISO 42001 for HR and staffing
- ISO 42001 certification in India
- ISO 42001 internal audit
- ISO 42001 management review
- ISO/IEC 42001 requirements explained, clause by clause
Keep exploring
Explore more about ISO/IEC 42001
Watch a video on how to implement ISO 42001 here.
Watch a video on ISO 42001 requirements here.
ISO/IEC 42001 resources
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