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For US manufacturers, machine shops, contractors & distributors · 5–100 staff

Audit-ready ISO 9001:2026 in 14 days.

Without the $8–15k consultant or the 3–6 month project.

Answer a 25-minute questionnaire. Our software generates your company-specific quality management system — about 36 documents, each mapped to an ISO 9001:2026 clause and checked by validators — plus the internal audit, management review and audit-day pack you need before the registrar walks in.

Questionnaire
25 min
Full draft QMS
48 h
Audit + review pack
Day 14
Documents, clause-mapped
~36
Price, fixed
$2,990

01The problem

Your customer just made ISO 9001 a condition of the contract.

It shows up as a line in a tender, a box on a supplier questionnaire you can't tick, or an email from purchasing: “please provide your ISO 9001 certificate.” You already run a good shop. What you don't have is the documented system an auditor needs to see.

The usual answer is a consultant. They're often good — but it's $8–15k, three to six months of meetings, and you still end up writing half of it yourself. Template packs are cheaper, then you spend weeks filling in blanks with text an auditor can tell wasn't written for you.

Meanwhile the contract has a date on it.

The consultant route, line by lineTypical US small-co.
QMS documentation$5,000–8,000
Implementation support & training$1,000–2,000
Outsourced internal audit$750+
Management review facilitation$500
Audit-prep coaching$1,000–2,000
Lead time3–6 months
All-in$8–15k

Registrar fees ($2.5–8k) are extra on every route — including ours.

02How it works

Four steps from “we need ISO 9001” to the registrar's Stage 2 audit.

  1. 01 · Day 0

    Answer the questionnaire

    25 minutes

    Your products, processes, machines, customers, suppliers and who signs off what. Upload existing SOPs, forms or an org chart if you have them — the software reuses what works.

  2. 02 · Within 48 h

    The software builds your QMS

    ~36 documents

    Every document is generated from your answers and mapped to its ISO 9001:2026 clause. Validators check every required item is present, cross-references resolve and no generic filler survives. You review, edit and approve each one in your account.

  3. 03 · Days 3–90

    Implement and check it

    Internal audit + review pack by day 14

    Follow the 90-day kit: train staff, start keeping records. Run the AI internal audit and the management review. Registrars expect to see the system running with some records before Stage 2 — the plan sequences that for you.

  4. 04 · Registrar

    Stage 1 and Stage 2 audits

    Audit-day pack

    Pick an accredited registrar with the shortlist and RFQ template. Walk in with an evidence index and the questions the auditor will ask, clause by clause. The registrar decides certification.

03What you get

Everything between “we need ISO 9001” and audit day. One bill of materials.

Audit-Ready ISO 9001:2026 System

  • 01

    Company-specific QMS

    Context & interested parties, scope, quality policy, objectives, process map, risk and opportunity registers, and procedures, forms and records — about 36 documents generated from your answers on ISO 9001:2026.

    Value: $5–8k · consultant documentation fee

  • 02

    90-day implementation kit

    Week-by-week rollout plan, staff awareness training (slides, quiz, sign-off records) and a starter set of records.

    Value: $1–2k

  • 03

    AI internal audit

    Clause-by-clause audit questionnaire with evidence upload. Produces an audit report with findings and corrective actions. Required before Stage 2.

    Value: $750–7.5k · per outsourced internal audit

  • 04

    Management review pack

    Agenda, required inputs and results minutes, auto-filled from your internal audit and objectives data.

    Value: $500

  • 05

    Audit-day pack

    Stage 1 and Stage 2 mock-audit Q&A, an evidence index, and “what the auditor will ask” for every clause.

    Value: $1–2k · audit-prep coaching

  • 06

    Registrar picker

    Shortlist of accredited certification bodies, an RFQ template and a quote-comparison sheet.

    Value: $1–3k · typical saving on registrar fees

  • 07

    AI QMS assistant — 12 months

    Ask anything about your system. Drafts new procedures and corrective actions in your house style.

    Value: $150/hr · consultant time equivalent

  • 08

    Kept current for year 1

    ISO 9001:2026 transition updates and new clause guidance pushed to your account.

    Value: Included

  • +

    Bonus: ISO 14001 / 45001 readiness check

    See how far your QMS is from an integrated quality + environmental or safety system.

    Value: Included

Total standalone value

$10–20k

Your price

$2,990one-time, 12 months' access included

or 3 monthly payments of $1,090

We onboard 40 companies a month so every account gets fast generation and support.

Versus

Consultant
$8–15k + 3–6 months
Templates you fill in
$200–2.5k + your weeks
QMSReady
$2,990 + 48 h draft

05Clause coverage

Every clause, 4 to 10, traced to a document you'll own.

Built to the ISO 9001:2026 requirements, including what changed from 2015. Plus the forms and record templates each procedure calls for: NCR, CAPA, training records, calibration log, supplier evaluation, audit checklist.

4

Context of the organization

2026: Climate change decision built into 4.1 / 4.2

  • Quality Manual QM-01 · 4.3, 4.4
  • Context of the Organization and Interested Parties QM-02 · 4.1, 4.2
  • Process Map and Process Interaction QM-03 · 4.4
  • 90-Day Implementation Plan IK-01 · 4.4
  • Audit-Day Pack IK-03 · 4.3
  • Registrar Selection and RFQ Pack IK-04 · 4.3

5

Leadership

2026: Quality culture & ethical behaviour (5.1.1)

  • Quality Manual QM-01 · 5.1.1
  • Quality Policy QP-01 · 5.2, 5.1.2
  • Organization, Roles, Responsibilities and Authorities QP-02 · 5.3, 5.1.1
  • Staff Awareness Training Pack IK-02 · 5.2

6

Planning

2026: 6.1 split into 6.1.1 / 6.1.2 / 6.1.3; stronger change control (6.3)

  • Quality Objectives and Plans QP-03 · 6.2
  • Risks and Opportunities Procedure and Register QP-04 · 6.1.1, 6.1.2, 6.1.3
  • Planning and Control of Changes QP-05 · 6.3
  • Change Request and Review Form F-10 · 6.3

7

Support

2026: Awareness now covers quality culture & ethics (7.3)

  • Quality Manual QM-01 · 7.5.1
  • Organization, Roles, Responsibilities and Authorities QP-02 · 7.1.2
  • Control of Documented Information QP-06 · 7.5.1, 7.5.2, 7.5.3
  • Competence, Training and Awareness QP-07 · 7.2, 7.3, 7.1.6
  • Monitoring and Measuring Equipment (Calibration) QP-08 · 7.1.5
  • Infrastructure, Maintenance and Work Environment QP-09 · 7.1.3, 7.1.4, 7.1.1
  • Communication QP-10 · 7.4
  • Training Record and Competence Matrix F-01 · 7.2
  • Calibration and Verification Log F-02 · 7.1.5
  • 90-Day Implementation Plan IK-01 · 7.3
  • Staff Awareness Training Pack IK-02 · 7.3

8

Operation

2026: Customer contingency & disruption communication (8.2.1)

  • Process Map and Process Interaction QM-03 · 8.1
  • Planning and Control of Changes QP-05 · 8.1, 8.5.6, 8.2.4
  • Communication QP-10 · 8.2.1
  • Customer Requirements and Contract Review QP-11 · 8.2.2, 8.2.3, 8.2.4, 8.2.1
  • Design and Development (if you design products/services) QP-12 · 8.3
  • Purchasing and External Provider Control QP-13 · 8.4.1, 8.4.2, 8.4.3
  • Production and Service Provision Control QP-14 · 8.5.1, 8.5.2, 8.5.3, 8.5.4, 8.5.5, 8.1
  • Inspection, Testing and Release QP-15 · 8.6, 8.5.1
  • Control of Nonconforming Outputs QP-16 · 8.7
  • Supplier Evaluation and Re-evaluation Form F-03 · 8.4.1
  • Contract and Order Review Checklist F-04 · 8.2.3
  • Nonconformance Report (NCR) F-05 · 8.7
  • Change Request and Review Form F-10 · 8.5.6

9

Performance evaluation

2026: Objectives for each audit (9.2.2); new review input (9.3.2)

  • Risks and Opportunities Procedure and Register QP-04 · 9.1.3
  • Monitoring, Measurement, Analysis and Customer Satisfaction QP-17 · 9.1.1, 9.1.2, 9.1.3
  • Internal Audit QP-18 · 9.2
  • Management Review QP-19 · 9.3.1, 9.3.2, 9.3.3
  • Internal Audit Plan, Checklist and Report F-07 · 9.2
  • Management Review Minutes F-08 · 9.3.2, 9.3.3
  • Customer Feedback and Satisfaction Survey F-09 · 9.1.2
  • 90-Day Implementation Plan IK-01 · 9.2, 9.3.1
  • Audit-Day Pack IK-03 · 9.2, 9.3.1

10

Improvement

2026: 2015's 10.1 and 10.3 merged into a new 10.1

  • Nonconformity, Corrective Action and Continual Improvement QP-20 · 10.2, 10.1
  • Corrective Action Request (CAR) F-06 · 10.2
  • Audit-Day Pack IK-03 · 10.2

06Guarantee

The documentation guarantee.

“If your accredited registrar raises a documentation nonconformity against anything our software generated, we fix it within 5 business days, free. If you fail Stage 2 because of our documentation, you get a full refund.”

Covered

Documentation findings against what the software generated, raised by an accredited registrar within 12 months of purchase. Plus a full refund within 14 days if you haven't generated any documents yet.

Not covered

Certification itself — your registrar decides that — and findings about implementation, records or training, which are yours to run.

Read the full refund policy and conditions →

07Compare

Three ways to get audit-ready.

CriterionConsultantTemplate packQMSReady
Price$8–15k$200–2,500$2,990 fixed, or 3 × $1,090
Time to complete documentation3–6 monthsAs long as it takes you48 hours to full draft
Your effortMeetings, site days, review cyclesYou write every section25-min questionnaire, then review & approve
Tailored to your company Generic Generated from your answers
Internal auditOften billed extra AI internal audit
Management reviewFacilitatedBlank template Auto-filled pack
Audit-day prepOften billed extra Per-clause Q&A + evidence index
Person on site Software — you implement

08Fit

Built for small US manufacturers. Not for everyone.

It's for you if

  • You're a manufacturer, machine shop, fabricator, contractor or distributor with 5–100 people.
  • A customer, prime contractor or tender now requires ISO 9001 — and there's a date attached.
  • You're going for ISO 9001 certification for the first time, or rebuilding an old QMS on the 2026 revision.
  • Someone on your team can own quality for a few hours a week.
  • You'd rather pay a fixed price for software than for consultant days.

It's not for you if

  • You make regulated medical devices and need ISO 13485.
  • You need AS9100 for aerospace — not supported yet.
  • You want someone on site running the project for you.
  • You want a certificate without implementing a system. No legitimate route offers that.

09Timing

Built on ISO 9001:2026 — no second transition before 2029.

  1. 16 Sep 2026

    ISO 9001:2026 published

    Your system is generated on the new revision from day one.

  2. 31 Mar 2028

    2026-only for new certifications

    From this date, new certifications are issued to ISO 9001:2026 only.

  3. 30 Sep 2029

    Transition ends

    The 3-year transition ends. Organizations holding 2015 certificates must have moved to 2026 by then.

10FAQ

Straight answers.

Still unsure? Email support@qmsready.com.

Are you a certification body?

No. QMSReady is software. We don't certify anyone, and no legitimate company can sell you a certificate without an audit.

Here's how certification actually works: an accredited certification body (a “registrar”, accredited by a body such as ANAB in the US or UKAS in the UK) audits you in two stages. Stage 1 reviews your documentation and readiness. Stage 2 checks on site that your system is implemented and working. If you pass, the registrar issues the certificate and returns for surveillance audits every year.

We give you the system and the preparation. You implement it. The registrar audits and decides. Typical registrar fees for a small company are $2.5–8k for Stage 1 + Stage 2, plus an annual surveillance audit.

What will the registrar cost on top?

Budget roughly $2.5–8k for the initial Stage 1 + Stage 2 audit, depending on headcount, number of sites and scope, plus a smaller surveillance audit each year and recertification every three years. Registrar fees are paid directly to the registrar and are not included in our price. The registrar picker includes an RFQ template so you can compare like-for-like quotes from accredited bodies. You can check any registrar's accreditation with the national accreditation body (ANAB in the US) or Global ACI.

How long does it take?

Your full draft QMS is generated within 48 hours of finishing the questionnaire. Most companies review and approve it within a week. The internal audit and management review pack is ready by day 14.

Registrars want evidence the system is running, so plan on roughly 3–4 months from purchase to Stage 2 for a small company. The 90-day implementation kit is built around that, and registrar availability is often the real bottleneck — book early.

Do I have to implement it myself?

Yes. The software generates the documents, plans and audit tools; your team runs the processes, keeps the records and trains staff. Auditors interview your people and look at real records, so nothing replaces that. The 90-day kit breaks implementation into weekly tasks, and the AI QMS assistant answers questions as you go. Expect the person who owns quality to spend a few hours a week on it.

We already have some procedures and forms. Do we start over?

No. Upload your existing SOPs, work instructions, forms and org chart. The software uses them as inputs, keeps what already reflects how you work, maps it to the 2026 clauses and generates only what's missing.

Will an auditor accept AI-generated documents?

Auditors don't care who typed a document. They care whether it describes what your company actually does, and whether your people follow it. Generic boilerplate is what gets flagged, so the software is built to prevent it:

  • We force company specifics. The questionnaire captures your real products, machines, customers, roles and numbers, and documents must use them.
  • Validators reject generic text. Documents that don't reference your specifics, miss a required item or break a cross-reference are regenerated before you see them.
  • Every document is reviewed and approved by you. Nothing becomes part of your QMS until your named approver signs it off in your account.

And if your registrar raises a documentation nonconformity against anything the software generated, the guarantee applies.

ISO 9001:2015 or 2026 — which should we build on?

2026. ISO 9001:2026 was published on 16 September 2026. From 31 March 2028, new certifications are issued to ISO 9001:2026 only, and the 3-year transition ends 30 September 2029. Building on 2026 now means no second transition before 2029.

ISO describes 2026 as an update, not a rewrite: the clause 4–10 structure is unchanged and most requirements are clarified rather than new. Your generated system covers the 2026 additions: quality culture and ethical behaviour (5.1.1, 7.3), risks and opportunities planned separately (6.1.1–6.1.3), stronger change management (6.3), the climate-change decision in context (4.1/4.2), customer contingency communication (8.2.1), objectives for each internal audit (9.2.2) and the new management-review input on interested-party changes (9.3.2).

Do we need a carbon or climate plan for ISO 9001:2026?

No. ISO 9001:2026 asks you to consider whether climate change is relevant to your quality management system and to record your decision and the reasoning. It doesn't require an environmental programme. The software prompts for the factors that matter to a shop (storm outages, shop temperature and tolerances, customer questionnaires) and writes the decision into your context register. See the sample.

What's your refund policy?

Full refund within 14 days if you haven't generated any documents yet. After that, the documentation guarantee applies: we fix any registrar documentation nonconformity against our generated documents within 5 business days, free, and refund you in full if you fail Stage 2 because of our documentation. Conditions are in the refund policy.

Can we pay in instalments?

Yes: 3 monthly payments of $1,090. You get the same system and access from day one. Choose the payment plan.

Is our data secure?

Your questionnaire answers and uploads are used only to generate and support your QMS. They're stored with our hosting provider and processed by our AI provider under commercial terms that don't allow your data to be used to train their models. We never sell your data, and we delete it on request. Details and the full list of processors are in the privacy policy.

Can I talk to someone first?

There are no sales calls — it's self-serve so we can keep the price fixed. Email support@qmsready.com with any question and you'll get a written answer, usually within one business day. Or take the free gap score first.

Your customer wants ISO 9001. Have the system drafted by the end of the week.

25-minute questionnaire. Full draft QMS in 48 hours. Internal audit and management review pack by day 14. $2,990 fixed, or 3 × $1,090. We onboard 40 companies a month.

Just want templates?

DIY Toolkit — $590

Clause-mapped template set plus the AI QMS assistant. You fill it in yourself — no tailoring, no internal audit. What you paid is credited toward the full system if you upgrade within 30 days.

Get the DIY Toolkit →

$2,990

or 3 × $1,090

Get audit-ready