Lean ISO 9001:2026 essentials, organized around the standard. Optional extras when you need them.
The essential quality documents for ISO 9001:2026, ready to adapt for your audit, in plain English, plus a step-by-step implementation guide. Optional extras are included as a bonus, not in your way.
Written for ISO 9001:2026 (published September 2026). This is not a 2015 kit with a promised upgrade.
Not on sale yet: free early access. The documents are written. Before launch, early access is free for up to 15 organizations in exchange for feedback, and one place can cover this kit and our kits for the other two standards. We may end or close early access at any time, without notice.
Core Kit
The essential documents and a step-by-step path to your audit.
US$490 at launchNot on sale yet · Free early access
- All the Essentials: scope, policy, gap-analysis checklist, risk and objectives registers, and the forms and registers that produce the records auditors check
- "Read Me First" step-by-step implementation guide: the Essentials in order, with a sample timeline you adapt to your organization
- Optional extras as a bonus: quality manual, 10 written procedures (each opens with a one-page flowchart), templates and extra registers
- 30 days of email support
- 12 months of updates
Implementation Kit
RecommendedEverything in Core, plus more optional extras and Implementation tools.
US$690 at launchNot on sale yet · Free early access
- Everything in the Core Kit
- Plus more optional extras:
- Gantt implementation project plan
- Annual QMS calendar and Stage 1 readiness tracker
- Editable process flowchart pack (PowerPoint), 2015-to-2026 transition guide and root cause analysis worksheet
- Implementation tools: staff awareness training deck, "What the auditor will ask" guide, management review pack and a fictional worked-example company pack
- 90 days of email support
- 12 months of updates
Planned launch prices in USD. Not on sale yet: no payment, no pre-order. Early-access copies are free and come with the Early Access License. The Integrated bundle will cover all three standards (planned launch price US$1,290). Not part of early access. Not on sale yet.
Step-by-step implementation path
Your step-by-step path to the certification audit
Read Me First, the kit's step-by-step implementation guide, takes you through the Essentials in order, with optional extras only if you want them. The certification decision is always made by your certification body, after its audit.
- 1
Check where you stand
Score yourself with the free Gap Analysis Checklist for ISO 9001:2026 (QMS-00-04, an Essential and also a free download).
- 2
Follow the step-by-step implementation guide
Read Me First (QMS-00-01) lists the Essentials in the order to complete them, the records auditors ask for at Stage 1 and Stage 2, and a sample timeline you adapt to your organization.
- 3
Set the foundations
Scope, context, interested parties, process map and quality policy (QMS-F-01, R-01, R-02, F-02, P-01).
- 4
Plan and run it
Risks and opportunities, objectives and changes (QMS-R-04, R-05, F-04), then the operational records: order review, suppliers, release and nonconforming output (QMS-F-09, R-12, F-12, F-13).
- 5
Check it yourself
Monitor KPIs (QMS-R-14), run a full internal audit (QMS-R-15, F-15, F-18), hold a management review (QMS-F-16) and log corrective actions (QMS-R-16).
- 6
Book your certification audit
With a certification body of your choice. The certification decision is theirs, after their audit.
New in the 2026 edition
What changed in ISO 9001:2026, and where the kit covers it
The biggest new requirement is quality culture and ethical behavior. The kit gives you a ready-to-adapt statement to evidence it, plus updated registers and procedures for the other changes.
Quality culture and ethical behavior · cl. 5.1.1, 7.1.4, 7.3
Quality culture and ethical behavior statement (QMS-P-02), leadership commitment evidence log (QMS-F-03) and induction and awareness briefing pack (QMS-F-06).
Risks and opportunities handled separately · cl. 6.1, 9.1.3
Risk and opportunity management procedure (QMS-PR-01) and a register with separate Risks and Opportunities tabs (QMS-R-04).
Interested parties and climate change · cl. 4.1, 4.2, 9.3.2
Context analysis register with a recorded climate-change decision (QMS-R-01) and interested parties register (QMS-R-02).
Planning of changes strengthened · cl. 6.3
Management of change procedure (QMS-PR-02) and change request and review form (QMS-F-04).
Already certified to ISO 9001:2015? · cl. 4–10
The Implementation Kit adds a transition guide (QMS-00-05): a plain-words change map and a checklist of what to update in your existing system.
Changes as reported by certification and accreditation bodies. Check them against your own copy of ISO 9001:2026.
What's included
The essentials first. Extras as a bonus.
- A lean Essentials set of core documents and records, organized around the standard's clauses
- Editable templates with guidance notes and sample wording
- Structured around the standard's published clauses, with a clause-to-document map to help you and your auditor find your way
- IMS-ready structure, so adding a second or third standard is straightforward
- Every procedure opens with a one-page "process at a glance" flowchart; the Implementation Kit adds editable PowerPoint versions of all 10, plus a process interaction map
- No macros. Standard Word, Excel and PowerPoint formats; Office and Google compatibility testing in progress.
- Email support (30 days Core, 90 days Implementation)
- 12 months of updates included
Who this kit is for
- SMEs that need ISO 9001 to win or keep contracts, without paying for a consultant
- Certified organizations moving from ISO 9001:2015 to 2026 (the Implementation Kit includes a 2015-to-2026 transition guide)
- Quality coordinators who have been handed the job with little ISO experience
Document list
The Essentials first, then the optional extras
Clause references are indicative and shown to help you navigate. The kit's clause-to-document map gives the full mapping.
25 essential + 33 optional documents, plus 6 Implementation tools. Everything is in the Core Kit unless marked “Implementation Kit only”.
The Essentials 25 documents · the core documents and records, organized around the standard's clauses
QMS-00-01Read Me First: step-by-step implementation guide
A step-by-step implementation path: the Essentials in the order to complete them, the records auditors ask for at Stage 1 and Stage 2, and a sample timeline you adapt to your organization.
Step-by-step implementation guideWordQMS-00-04Gap analysis checklist with scoring dashboard
Also a free downloadThe same workbook as the free gap-analysis checklist, shipped in the kit as QMS-00-04: clause-by-clause scoring, readiness dashboard and flagged 2026 changes.
Your baseline before you startExcelQMS-F-01QMS scope statement
Cl. 4.3WordQMS-R-01Context analysis register (incl. climate change decision)
Cl. 4.1ExcelQMS-R-02Interested parties register
Cl. 4.2ExcelQMS-F-02Process map and turtle diagrams
Cl. 4.4ExcelQMS-P-01Quality policy
Cl. 5.2WordQMS-R-04Risk and opportunity register
Cl. 6.1ExcelQMS-R-05Quality objectives and action plan
Cl. 6.2ExcelQMS-F-04Change request and review form
Cl. 8.5.6WordQMS-R-07Monitoring and measuring equipment calibration register
Only needed if you use measurement to verify conformity
Cl. 7.1.5ExcelQMS-R-09Training matrix and competence register
Cl. 7.2ExcelQMS-R-11Master document list and retention schedule
Cl. 7.5.1, 7.5.3ExcelQMS-F-09Contract and order review checklist
Cl. 8.2.3WordQMS-F-10Design and development plan and record
Only needed if you design products or services
Cl. 8.3.2 to 8.3.6ExcelQMS-R-12Approved supplier list and evaluation
Cl. 8.4.1ExcelQMS-R-13Traceability and customer property log
Only needed where applicable: traceability where it is a requirement, and customer or provider property
Cl. 8.5.2, 8.5.3ExcelQMS-F-12Inspection and release record
Cl. 8.6ExcelQMS-F-13Nonconforming output report
Cl. 8.7.2WordQMS-R-14KPI monitoring and analysis dashboard
Cl. 9.1.1ExcelQMS-R-15Internal audit program
Cl. 9.2.2ExcelQMS-F-15Internal audit plan, checklist and report
Cl. 9.2.2WordQMS-F-18Internal audit checklist (clause by clause)
111 prompts with where to look, evidence sighted and OK / OFI / NC / NA ticks, 2026 items flagged, plus a process-audit variant that traces the record chain.
Cl. 9.2 (audit evidence)WordQMS-F-16Management review agenda and minutes
Cl. 9.3.3WordQMS-R-16NCR, CAPA and complaints register
Cl. 10.2.2Excel
Optional extras 33 documents · a bonus, use them if you want to go further
QMS-00-02Clause cross-reference matrix
Use it if: you want a clause-by-clause map of every document (useful for integration or a consultant review)
Cl. 4–10ExcelQMS-00-03Implementation project plan
Implementation Kit onlyUse it if: you want a dated Gantt plan; the Read Me First timeline is enough for most small businesses
ExcelQMS-00-05Transition guide: ISO 9001:2015 to 2026
Implementation Kit onlyUse it if: you are already certified to ISO 9001:2015 and are moving to the 2026 edition
Cl. AllWordQMS-R-19Annual QMS calendar and Stage 1 readiness tracker
Implementation Kit onlyUse it if: you want a year-round calendar of recurring activities and a scored Stage 1 readiness checklist
Cl. 9.2, 9.3, 7.5ExcelQMS-M-01Quality manual
Use it if: a customer or tender asks for a quality manual (not required by the standard)
Cl. 4–10WordQMS-F-19Process flowchart pack (PowerPoint)
Implementation Kit onlyUse it if: you want editable flowcharts of every procedure and an interaction map
Cl. 4.4, 8.1PowerPointQMS-P-02Quality culture and ethical behavior statement
Use it if: you want a separate statement on quality culture and ethical behavior (5.1.1, 7.1.4, 7.3); the policy and briefing can cover it
Cl. 5.1.1, 7.1.4, 7.3WordQMS-F-03Leadership commitment evidence log
Use it if: you want a running log of leadership evidence for 5.1
Cl. 5.1ExcelQMS-R-03Roles, responsibilities and authorities matrix
Use it if: you want a RACI matrix and role descriptions (5.3 requires roles to be assigned and communicated, not documented)
Cl. 5.3ExcelQMS-PR-01Risk and opportunity management procedure
Use it if: you want a written risk and opportunity method (the register's criteria sheet is enough for most)
Cl. 6.1, 9.1.3WordQMS-PR-02Management of change procedure
Use it if: you want a written change procedure (F-04 already records each change)
Cl. 6.3, 8.1, 8.5.6WordQMS-R-06Infrastructure and maintenance register
Use it if: you want an asset and maintenance register (7.1.3)
Cl. 7.1.3ExcelQMS-R-08Organizational knowledge register
Use it if: you want to record critical knowledge and handovers (7.1.6)
Cl. 7.1.6ExcelQMS-PR-03Competence, training and awareness procedure
Use it if: you want a written competence and awareness procedure (R-09 holds the evidence)
Cl. 7.2, 7.3WordQMS-F-05Training record and effectiveness evaluation
Use it if: you want a separate training record with an effectiveness check (R-09 can hold the evidence references)
Cl. 7.2WordQMS-F-06Induction and awareness briefing pack
Use it if: you want ready-to-deliver induction and awareness briefing notes (7.3)
Cl. 7.3, 5.2WordQMS-R-10Communication plan
Use it if: you want a written communication plan (7.4)
Cl. 7.4ExcelQMS-F-20Team meeting minutes and attendance
Use it if: you want a standard team or toolbox meeting record
Cl. 7.4, 7.3, 5.1.1WordQMS-PR-04Control of documented information procedure
Use it if: you want a written document control procedure
Cl. 7.5WordQMS-F-07Document template
Use it if: you want a standard template for new documents
Cl. 7.5.2WordQMS-PR-05Operational planning and control procedure
Use it if: you want a written operational planning and control procedure
Cl. 8.1, 8.5WordQMS-F-08Work instruction template (with worked example)
Use it if: you want a work instruction format
Cl. 8.5.1WordQMS-PR-06Customer requirements and communication procedure
Use it if: you want a written customer requirements procedure
Cl. 8.2WordQMS-PR-07Design and development procedure (use if applicable)
Use it if: you design and want a written design procedure (F-10 holds the records)
Cl. 8.3WordQMS-PR-08Purchasing and external provider control procedure
Use it if: you want a written purchasing procedure
Cl. 8.4WordQMS-F-11Purchase order requirements template
Use it if: you want a standard list of requirements for purchase orders (8.4.3)
Cl. 8.4.3WordQMS-F-21Supplier prequalification questionnaire
Use it if: you want a supplier pre-qualification questionnaire for higher-risk suppliers
Cl. 8.4.1, 8.4.2WordQMS-R-18Statutory, regulatory and customer requirements register
Use it if: you want a separate register of legal and customer requirements
Cl. 8.2.2, 5.1.2, 4.2ExcelQMS-F-14Customer satisfaction survey and feedback log
Use it if: you want a customer satisfaction survey and feedback log (9.1.2; results can go in R-14)
Cl. 9.1.2ExcelQMS-PR-09Internal audit procedure
Use it if: you want a written internal audit procedure (R-15, F-15 and F-18 hold the records)
Cl. 9.2WordQMS-PR-10Nonconformity and corrective action procedure
Use it if: you want a written nonconformity procedure (R-16 holds the records)
Cl. 10.2, 8.7WordQMS-R-17Continual improvement register
Use it if: you want an improvement register and change log (10.1)
Cl. 10.1, 6.1.3ExcelQMS-F-17Root cause analysis worksheet (5 Whys and fishbone)
Implementation Kit onlyUse it if: you want a guided 5 Whys / fishbone worksheet
Cl. 10.2Word
Implementation tools Implementation Kit only · not counted in the kit documents
Documents (6)
QMS-IMP-01Quality awareness training deck
24-slide all-staff session with speaker notes on every slide and a 5-question quiz, including quality culture, ethics and risks and opportunities (2026).
Cl. 7.3, 5.1.1PowerPointQMS-IMP-02"What the auditor will ask" guide
For each clause: typical questions, who is usually asked, the evidence to show (linked to kit documents) and common pitfalls. Plus an on-the-day checklist.
Cl. 4–10WordQMS-IMP-03Worked example pack: fictional example company (8 files)
Completed documents for "Brindlemoor Enclosures Ltd", an invented manufacturer: profile, policy, context, interested parties, risk and opportunity registers, objectives, CAPA procedure and review minutes. Every page is marked FICTIONAL EXAMPLE.
Cl. 4.1–10.2WordQMS-IMP-04Management review agenda and input/output checklist
Timed agenda and a checklist of the review inputs, with source document, preparer and Ready/Covered ticks.
Cl. 9.3WordQMS-IMP-05Management review minutes template (extended)
Extends QMS-F-16 with previous actions, a decisions log, an action plan and distribution.
Cl. 9.3WordQMS-IMP-06Management review presentation template (12 slides)
Slides for presenting the inputs, with risks and opportunities on separate slides and speaker notes naming each source.
Cl. 9.3PowerPoint
Document numbers match the files in the kit. Wording may still be refined before release (a final check against the published standard and a professional proofread are pending).
Sample preview
Look inside before you buy
These are real pages from the kit, and each one is marked. Any document still being finalized shows its planned contents instead.
Real page from this kit
Implementation project plan, from kick-off to certification audit
Every task is linked to its clause and to the kit document that covers it, with owners, dates and a weekly Gantt chart. Set your start date and the plan fills itself in.
Included in the Implementation Kit.
Want to try it first? The free Gap Analysis Checklist for ISO 9001:2026 is the same workbook that ships in the Core Kit as QMS-00-04.
Get the free checklistDetails
Formats, license and support
- Formats
- Word (.docx) and Excel (.xlsx), plus PowerPoint (.pptx) in the Implementation Kit. No macros. Standard Word, Excel and PowerPoint formats; Office and Google compatibility testing in progress. The PowerPoint files are standard 16:9 .pptx files with no macros.
- License
- One organization, unlimited users, all sites. No resale. Consultants: see the Consultant License.
- Support
- Email support: 30 days (Core) or 90 days (Implementation).
- Delivery
- Instant download link after purchase (once checkout opens).
FAQ
Common questions
Will this kit guarantee that we get certified?
Do I still need to buy the ISO standard itself?
What formats do the documents come in?
What is the difference between the Core Kit and the Implementation Kit?
What license do I get?
How do you keep the kits aligned with the standard?
Do I get updates?
Going integrated?
Quality, environment and safety in one system, planned at US$1,290.