Home β€Ί Documentation Kits β€Ί ISO 56001:2024
Innovation Management Systems Β· ISO 56001:2024

ISO 56001:2024 Documentation Toolkit

The real ISO 56001:2024 documentation set we deliver: 187 documents and six ready-to-use Excel tools that form a complete innovation management system (IMS), the first innovation standard you can certify to. The manual maps every clause of ISO 56001:2024 to the procedure that implements it, and each procedure carries its own clause annex. You get the IMS Manual, Innovation Policy, 20 procedures, 6 work instructions, 76 forms each with a completed worked example, and the portfolio, risk, idea-scoring, KPI, competence and IP tools, all editable in Word and Excel, so you can build a certification-ready innovation system without hiring a consultant.

187
Documents
and tools
20
Procedures
clause-mapped
76
Forms with
filled samples
6
Validated
Excel tools
$149
βœ“ Within 24h secure deliveryβœ“ Editable Word and Excelβœ“ Lifetime free updates
ISO 56001:2024MANUAL
Innovation Management Systems System Manual
Clause-by-clause structure
20Clause-mapped
procedures
76Ready-to-use
forms
Written to satisfy the requirements checked byBSISGSTÜVBureau VeritasDNVIntertek
Overview

Everything you need for ISO 56001:2024, in one download

Preparing the documentation is the slowest and most confusing part of getting certified to ISO 56001:2024. 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 56001:2024 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 innovation 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

The first certifiable innovation standard

ISO 56001:2024 is the first innovation management system standard an organisation can be certified against, where earlier innovation standards were guidance only. This set is written to its requirements, clause by clause, so you build a system a certification body will recognise.

Every clause mapped to its procedure

The manual maps every requirement of clauses 4 to 10 to the procedure that implements it, and each procedure carries an annex mapping its owned clauses to its sections, so you can trace any requirement to its evidence.

The full innovation process, opportunities to deployment

A dedicated procedure and ten forms carry an idea from opportunity and insight, through concept, assumption testing and validation, to deployment and value realisation, with initiative charters and gate decisions along the way.

Portfolio, IP and strategic intelligence

Beyond the core clauses, the set covers innovation portfolio management, intellectual property aligned to ISO 56005, and the strategic intelligence and insight work that feeds the funnel, each with its own procedure, forms and tools.

A completed example for every form

All 76 forms come with a matching sample filled form, worked around a realistic software-company example, so you can see exactly how each record should look before you fill your own.

Six ready-to-use Excel tools

Working tools with the formulas already in place, for portfolio scoring and balancing, the risk and opportunity register, the innovation KPI dashboard, idea and concept scoring, the competence matrix and the IP inventory.

How the set is structured

187 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.

MAN1Innovation Management System Manual
POL1Innovation Policy
QP20Procedures
WI6Work instructions
QF76Forms and registers
SMP76Sample filled forms
TOOL6Validated Excel tools
CUST1Customization and implementation guide
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 56001:2024 Toolkit

A complete document set, fully editable in Microsoft Office.

Innovation Management System Manual1
Innovation Policy1
Procedures20
Work instructions6
Forms and registers76
Sample filled forms76
Validated Excel tools6
Customization and implementation guide1
Total documents187

MAN-01 Innovation Management System Manual

The top-level document of the IMS and the entry point to the whole set. It demonstrates, clause by clause, how the organisation meets ISO 56001:2024, states the innovation management model behind the system, and traces every requirement to the procedure, form, tool and record that provides evidence. An annex maps every clause to its documents. This is the document an auditor opens first.

Introduction and organisation overviewScope, references and the ISO 5600x family4. Context of the organisation5. Leadership and innovation policy6. Planning: risks, opportunities and objectives7. Support: people, resources, knowledge, IP8. Operation: the innovation process9. Performance evaluation10. ImprovementAnnexes: process map, clause matrix, KPIs
POL Innovation Policy (1)
  • POL-01 Innovation Policy. Top management commitment to innovation: the intent, principles and objectives that direct the innovation management system, aligned to ISO 56001 Clause 5.2.
QP Procedures (20)
  • QP-01 Context, Interested Parties and Scope. How the organisation determines its context, its interested parties and their needs, and sets the scope of the IMS (Clause 4).
  • QP-02 Innovation Intent, Strategy and Culture. How the organisation sets its innovation intent and strategy and builds a culture that supports innovation.
  • QP-03 Managing Risks and Opportunities. How risks and opportunities to the IMS and to innovation are identified, assessed and treated (Clause 6.1).
  • QP-04 Innovation Objectives and Planning. How innovation objectives are set, planned and monitored (Clause 6.2).
  • QP-05 Innovation Portfolio Management. How the mix of innovation initiatives is entered, reviewed and balanced against strategy and risk.
  • QP-06 Organizational Structures and Collaboration. How innovation structures are defined and how internal and external collaboration and partnerships are managed.
  • QP-07 Competence, Awareness and Training. How competence is defined and built, awareness is maintained and training is delivered (Clause 7.2, 7.3).
  • QP-08 Innovation Resources. How the people, time, funding and infrastructure that innovation needs are planned and provided (Clause 7.1).
  • QP-09 Knowledge and Intellectual Property Management. How knowledge and intellectual property are captured, protected and exploited, aligned to ISO 56005.
  • QP-10 Innovation Tools and Methods. How innovation tools and methods are selected, registered and taught.
  • QP-11 Communication. How internal and external communication about innovation is planned and recorded (Clause 7.4).
  • QP-12 Control of Documented Information. How IMS documents and records are created, approved, issued, changed and controlled (Clause 7.5).
  • QP-13 Operational Planning and Control. How innovation operations are planned and controlled, including externally provided processes (Clause 8.1).
  • QP-14 Innovation Initiative Management. How an individual innovation initiative is chartered, resourced, gated and closed with lessons captured.
  • QP-15 Innovation Process (Opportunities to Deployment). The core innovation funnel: how opportunities and ideas become validated concepts and then deployed, value-realising solutions (Clause 8.2).
  • QP-16 Monitoring, Measurement, Analysis and Evaluation. How IMS performance and innovation results are monitored and evaluated against indicators (Clause 9.1).
  • QP-17 Internal Audit. How internal audits of the IMS are planned, conducted and reported (Clause 9.2).
  • QP-18 Management Review. How top management reviews the IMS and sets actions (Clause 9.3).
  • QP-19 Continual Improvement and Corrective Action. How nonconformities are handled, corrective action is taken and improvement is driven (Clause 10).
  • QP-20 Change Management. How changes to the IMS and to innovation activities are requested, assessed and implemented.
WI Work instructions (6)
  • WI-05-01 Portfolio Scoring and Balancing. Step-by-step method for scoring and balancing the innovation portfolio, using the portfolio workbook.
  • WI-09-01 IP Search and Disclosure. How to run an intellectual property search and record a disclosure.
  • WI-15-01 Opportunity Identification Sprint. How to run a sprint that identifies and frames innovation opportunities.
  • WI-15-02 Idea and Concept Screening. How to screen ideas and concepts using the scoring matrix.
  • WI-15-03 Assumption Testing and Experiment Design. How to design an experiment and test the assumptions behind a concept.
  • WI-17-01 Conducting an Internal Audit. How to plan, run and report an internal audit of the IMS.
QF Forms and registers (76)
  • QF-01-01 Context and Issues Analysis. Records the internal and external issues that shape the IMS.
  • QF-01-02 Interested Parties and Requirements Register. Records interested parties and their relevant requirements.
  • QF-01-03 Areas of Opportunity Register. Records the broad areas where the organisation could innovate.
  • QF-01-04 IMS Scope Statement. States the boundaries and applicability of the IMS.
  • QF-02-01 Innovation Intent Statement. Sets out the organisation intent to innovate and why.
  • QF-02-02 Innovation Strategy Record. Records the innovation strategy that pursues the intent.
  • QF-02-03 Innovation Culture Assessment. Assesses the organisation culture for innovation.
  • QF-03-01 Risk and Opportunity Register. Records risks and opportunities to the IMS and to innovation.
  • QF-03-02 Risk and Opportunity Action Plan. Plans and tracks actions on risks and opportunities.
  • QF-04-01 Innovation Objectives Register. Records the innovation objectives and their targets.
  • QF-04-02 Objective Achievement Plan. Plans how each objective will be achieved.
  • QF-04-03 Objective Monitoring Record. Tracks progress against the objectives.
  • QF-05-01 Initiative Intake and Portfolio Entry. Captures a new initiative and enters it into the portfolio.
  • QF-05-02 Portfolio Review Record. Records a review of the innovation portfolio.
  • QF-05-03 Portfolio Balance Report. Reports the balance of the portfolio across horizons and risk.
  • QF-06-01 Organizational Structure Definition. Defines the structures that support innovation.
  • QF-06-02 Collaboration Agreement Record. Records an agreement with an innovation partner.
  • QF-06-03 Collaboration Partner Evaluation. Evaluates a potential or current collaboration partner.
  • QF-07-01 Competence Requirements Definition. Defines the competencies that innovation roles need.
  • QF-07-02 Training Needs Analysis. Identifies the training needed to close competence gaps.
  • QF-07-03 Annual Training Plan. Plans the year innovation training.
  • QF-07-04 Training Attendance Record. Records who attended each training.
  • QF-07-05 Training Effectiveness Evaluation. Evaluates whether training was effective.
  • QF-07-06 Awareness Briefing Record. Records innovation awareness briefings to staff.
  • QF-07-07 Competence Matrix. Maps roles against the competencies they need.
  • QF-08-01 Resource Requirements Plan. Plans the resources that innovation needs.
  • QF-08-02 Innovation Funding Request. Requests funding for an innovation initiative.
  • QF-08-03 Time Allocation Record. Records the time allocated to innovation work.
  • QF-08-04 Infrastructure Register. Registers the infrastructure supporting innovation.
  • QF-09-01 Knowledge Asset Register. Registers the organisation innovation knowledge assets.
  • QF-09-02 Lessons Learned Record. Captures lessons learned from innovation work.
  • QF-09-03 IP Disclosure Form. Records a disclosure of potential intellectual property.
  • QF-09-04 IP Inventory. Inventories the organisation intellectual property.
  • QF-09-05 IP Ownership Agreement Record. Records agreements on the ownership of IP.
  • QF-10-01 Tools and Methods Register. Registers the innovation tools and methods in use.
  • QF-10-02 Method Training Record. Records training on innovation methods.
  • QF-11-01 Communication Plan. Plans internal and external innovation communication.
  • QF-11-02 Communication Record. Records innovation communications made.
  • QF-12-01 Master Document Register. The master index of every controlled IMS document.
  • QF-12-02 Document Change Request. Requests and records a change to a controlled document.
  • QF-12-03 Distribution List. Records who holds controlled copies of documents.
  • QF-12-04 External Documents Register. Registers documents of external origin used by the IMS.
  • QF-13-01 Operational Plan. Plans the operational innovation work for a period.
  • QF-13-02 Change Control Record. Records control of a change to operations.
  • QF-13-03 Externally Provided Process Control Record. Records control of processes provided by external parties.
  • QF-14-01 Innovation Initiative Charter. Charters an innovation initiative with its aim and scope.
  • QF-14-02 Initiative Gate Decision Record. Records a go, hold or stop decision at an initiative gate.
  • QF-14-03 Initiative Resource and Roles Assignment. Assigns resources and roles to an initiative.
  • QF-14-04 Initiative Closure and Lessons Report. Closes an initiative and captures its lessons.
  • QF-15-01 Opportunity Statement. States an innovation opportunity to pursue.
  • QF-15-02 Insight Log. Logs insights that could feed innovation.
  • QF-15-03 Idea Capture Form. Captures an idea and the opportunity it responds to.
  • QF-15-04 Concept Brief and Value Proposition. Describes a concept and the value it would create.
  • QF-15-05 Assumption and Uncertainty Log. Logs the assumptions and uncertainties behind a concept.
  • QF-15-06 Experiment and Test Card. Designs an experiment to test a key assumption.
  • QF-15-07 Concept Validation Report. Reports whether a concept was validated.
  • QF-15-08 Solution Development Record. Records the development of a validated concept into a solution.
  • QF-15-09 Deployment Plan. Plans the deployment of a solution.
  • QF-15-10 Deployment and Value Realization Review. Reviews deployment and the value the solution realised.
  • QF-16-01 Performance Indicator Definition. Defines an innovation performance indicator.
  • QF-16-02 Monitoring and Measurement Plan. Plans how performance is monitored and measured.
  • QF-16-03 Analysis and Evaluation Report. Reports the analysis and evaluation of performance.
  • QF-17-01 Annual Audit Programme. Plans the internal audit programme for the year.
  • QF-17-02 Audit Plan. Plans a single internal audit.
  • QF-17-03 Audit Checklist. The checklist used to audit the IMS.
  • QF-17-04 Audit Report. Reports the findings of an internal audit.
  • QF-17-05 Nonconformity Report. Records a nonconformity found in the IMS.
  • QF-17-06 Auditor Competence Evaluation. Evaluates the competence of an internal auditor.
  • QF-18-01 Management Review Agenda. The agenda for a management review.
  • QF-18-02 Management Review Input Pack. The inputs assembled for a management review.
  • QF-18-03 Management Review Minutes and Actions. Records the management review decisions and actions.
  • QF-19-01 Nonconformity and Corrective Action Request. Raises a nonconformity and requests corrective action.
  • QF-19-02 Continual Improvement Register. Registers continual improvement actions.
  • QF-19-03 Corrective Action Effectiveness Review. Reviews whether a corrective action worked.
  • QF-20-01 Change Request and Impact Assessment. Requests a change and assesses its impact.
  • QF-20-02 Change Implementation and Review Record. Records the implementation and review of a change.
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 76 additional worked examples included in the set.
TOOL Validated Excel tools (6)
  • T-01 Innovation Portfolio Scoring and Balancing Workbook. Scores and balances the innovation portfolio across horizons and risk.
  • T-02 Risk and Opportunity Register. Working register that scores risks and opportunities and tracks actions.
  • T-03 Innovation Performance Indicator Dashboard. Tracks the innovation KPIs and shows performance at a glance.
  • T-04 Idea and Concept Scoring Matrix. Scores ideas and concepts against defined criteria.
  • T-05 Competence Matrix. Scores competence against roles and highlights the gaps.
  • T-06 Intellectual Property Inventory Register. Inventories and tracks the organisation intellectual property.
CUST Customization and implementation guide (1)
  • Customization and Implementation Guide. How to tailor and implement the whole toolkit, with the placeholder replacement guide and the configuration decision checklist in one document.
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 56001:2024 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 56001:2024 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 56001:2024 toolkit, frequently asked

What is ISO 56001 and how is it different from ISO 56002?+
ISO 56001:2024 is the requirements standard for an innovation management system, published in September 2024, and it is the first innovation standard an organisation can be certified against. ISO 56002 and the rest of the ISO 5600x family give guidance; ISO 56001 sets the auditable requirements. This toolkit is written to ISO 56001:2024 and draws on the wider family where it helps.
Can any organisation use it, or only technology companies?+
The requirements of ISO 56001 are generic and apply to any organisation, of any size or sector. This toolkit is written around a realistic software-company example so that every section is filled and usable, and you replace that example with your own context, offerings and processes.
Does it cover the whole innovation process?+
Yes. A dedicated procedure and ten forms carry an idea from opportunity and insight through concept, assumption testing and validation to deployment and value realisation, and the portfolio procedure manages the mix of initiatives. Intellectual property, strategic intelligence and collaboration are covered by their own procedures.
Does every form come with a filled example?+
Yes. All 76 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.
Is it ready to certify as delivered?+
No template is. The set is a complete, clause-referenced starting point written for an example organisation. You replace the placeholders, make a small number of configuration decisions, and adapt the example content to your operations, then have a competent person review the tailored system before you seek certification.
What does the ISO 56001:2024 toolkit include?+
A clause-by-clause ISO 56001:2024 manual, 20 procedures, and 76 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 56001:2024 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 56001:2024 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 56001:2024 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

Frequently bought together

Get your ISO 56001:2024 system, ready today

Download the complete, editable toolkit and start building an audit ready system in minutes, with a free sample available before you buy.

ISO 56001:2024 Documentation Toolkit 187 documents, Word and Excel, delivery within 24 working hours $149