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Quality Management Β· ISO 9001:2015

ISO 9001:2015 Documentation Toolkit

The real ISO 9001:2015 documentation set: 79 documents that form a complete quality management system (QMS). The Quality Manual answers every clause of ISO 9001:2015, and you get 13 procedures, 8 process flow charts, 51 forms and formats and 6 exhibits and plans, covering context, leadership, planning, operation, purchasing, production, quality control, design and development, internal audit and management review, all editable in Word, so a company can build a certification-ready quality system without hiring a consultant.

79
Documents
and formats
13
Procedures
clause-mapped
51
Forms and
formats
8
Process
flow charts
$149
βœ“ Within 24h secure deliveryβœ“ Editable Word and Excelβœ“ Lifetime free updates
ISO 9001:2015MANUAL
Quality Management System Manual
Clause-by-clause structure
13Clause-mapped
procedures
51Ready-to-use
forms
Written to satisfy the requirements checked byBSISGSTÜVBureau VeritasDNVIntertek
Overview

Everything you need for ISO 9001:2015, in one download

Preparing the documentation is the slowest and most confusing part of getting certified to ISO 9001:2015. 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 9001:2015 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 quality management 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

A manual that answers every clause

The Quality Manual is written clause by clause against ISO 9001:2015, from context and leadership through planning, operation and performance evaluation to improvement, so an auditor can trace each requirement to where you meet it.

The process approach, drawn out

Eight process flow charts map customer service, marketing, purchasing, production, stores, quality control, engineering and research and development, so your QMS is shown as connected processes, exactly as ISO 9001:2015 expects.

Design and development covered

A full set of design forms, including R&D request and plan, design verification, review, monitoring register and experiment data sheet, so clause 8.3 is handled properly if it applies to you.

Purchasing, production and quality control

Procedures and forms for purchasing and subcontracting, incoming inspection, production planning, in-process and finished-product testing, nonconforming product and product recall, so the operational core is ready to run.

Audit and review, ready to go

Internal audit procedure with audit plan, checklist and report, plus management review agenda and minutes and a corrective action report, so the check-and-act half of the cycle is complete.

Competence and documents controlled

Skill matrix, competence gap analysis, training programme and records, plus master document lists, change notes and a management-of-change plan, so people and documents stay under control.

How the set is structured

79 controlled documents in 5 tiers

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

MAN1Quality Management System Manual
QP13Procedures
FLOW8Process flow charts
F51Forms and formats
EXH6Exhibits and plans
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 9001:2015 Toolkit

A complete document set, fully editable in Microsoft Office.

Quality Management System Manual1
Procedures13
Process flow charts8
Forms and formats51
Exhibits and plans6
Total documents79

M-01 Quality Management System Manual

The top-level document of the quality management system. It shows, clause by clause, how the organisation meets ISO 9001:2015, from context, leadership and the quality policy through planning, support, operation and performance evaluation to improvement, and links each requirement to the procedure, process, form and record that satisfies it.

Introduction and organisation structureApplicability and scope of the QMSNormative references, terms and definitions4. Context of the organisation5. Leadership and the quality policy6. Planning: risks, objectives and change7. Support8. Operation9. Performance evaluation10. Improvement
QP Procedures (13)
  • 01 Context of the Organization. How the organisation determines its context, interested parties and the scope of the QMS (Clause 4).
  • 02 Objectives and Targets. How quality objectives and targets are set and tracked (Clause 6.2).
  • 03 Monitoring and Measurement. How processes, product and satisfaction are monitored and measured (Clause 9.1).
  • 04 Management Review. How top management reviews the QMS (Clause 9.3).
  • 05 Internal Audit. How internal audits are planned and conducted (Clause 9.2).
  • 06 Training, Awareness and Competence. How competence, training and awareness are managed (Clause 7.2, 7.3).
  • 07 Control of Documents and Records. How documented information is controlled (Clause 7.5).
  • 08 Correction and Corrective Action. How nonconformities are corrected (Clause 10.2).
  • 09 Control of Monitoring and Measuring Equipment. How measuring equipment is controlled and calibrated (Clause 7.1.5).
  • 10 Purchasing and Subcontracting. How externally provided processes, products and services are controlled (Clause 8.4).
  • 11 Change Management. How changes to the QMS and processes are planned and controlled (Clause 6.3).
  • 12 Legal Compliance. How legal and other requirements are identified and evaluated.
  • 13 Control of Nonconforming Products. How nonconforming outputs are identified and controlled (Clause 8.7).
FLOW Process flow charts (8)
  • Customer Service Process Flow Chart. Maps the customer service process.
  • Dispatch Process Flow Chart. Maps the dispatch process.
  • Engineering Process Flow Chart. Maps the engineering process.
  • Marketing Process Flow Chart. Maps the marketing process.
  • Production Process Flow Chart. Maps the production process.
  • Stores Process Flow Chart. Maps the stores process.
  • Quality Control Process Flow Chart. Maps the quality control process.
  • Research and Development Process Flow Chart. Maps the research and development process.
F Forms and formats (51)
  • Packing Report / Slip. Records packing of product.
  • Drum, Bag and Carton Inspection Report. Records inspection of drums, bags and cartons.
  • Screen Checking Report. Records screen checking.
  • Breakdown History Card. Records equipment breakdown history.
  • Preventive Maintenance Schedule. Schedules preventive maintenance.
  • Preventive Maintenance Check Points. Checks preventive maintenance points.
  • Preventive Maintenance Check Points for Building and Facility. Checks building and facility maintenance.
  • Order Form / Order Confirmation. Confirms an order.
  • Customer Complaint Report. Records customer complaints.
  • Customer Feedback Form. Captures customer feedback.
  • Production Plan. Plans production.
  • Disposal of Nonconforming Products. Records disposal of nonconforming products.
  • Purchase Order. Raises a purchase order.
  • Indent and Incoming Inspection Record. Records indents and incoming inspection.
  • Approved Vendor List. Lists approved vendors.
  • Supplier Registration Form. Registers a supplier.
  • Sample Test Request Slip - In-Process / Finished Product. Requests testing of in-process or finished product.
  • Product Recall Report. Records a product recall.
  • Product Description Form. Describes a product.
  • Management Review Meeting Agenda. The agenda for a management review.
  • Management Review Meeting Minutes. Records management review decisions.
  • Corrective Action Report. Records corrective actions.
  • Master List of Records. The master index of records.
  • Objectives and Targets. Sets quality objectives and targets.
  • Audit Plan. Plans an internal audit.
  • Master List of Equipment. Registers equipment.
  • Document Change Note. Records a document change.
  • Training Attendance Sheet. Records attendance at training.
  • Employee Training and Competence Record Sheet. Records employee training and competence.
  • Performance Appraisal Report. Records performance appraisals.
  • Pest Control Report. Records pest control.
  • Research and Development Request Report. Requests R&D work.
  • Research and Development Plan. Plans R&D work.
  • Design Verification Report. Records design verification.
  • Design and Development Monitoring Register. Monitors design and development.
  • Design Review Report. Records a design review.
  • Experiment Data Sheet. Records experiment data.
  • Design Review Minutes of Meeting. Records design review minutes.
  • Gate Pass. Issues a gate pass.
  • Competence Matrix. Maps competence across roles.
  • Competence Gap Analysis Form. Analyses gaps in competence.
  • Annual Training Program. Plans the year training.
  • Induction Training Form. Records induction training.
  • Job Description. Defines a role and its responsibilities.
  • Master List of Documents. The master index of documents.
  • Management of Change Plan. Plans and controls a change.
  • Internal Audit Checklist. The checklist used to audit the QMS.
  • Internal Audit Report. Reports the findings of an internal audit.
  • Daily Stock Statement. Records the daily stock statement.
  • Customer Property Monitoring Register. Monitors customer property.
  • Visitor Entry Report. Records visitor entry.
EXH Exhibits and plans (6)
  • Skill Requirements. Defines the skill requirements for roles.
  • Multi-Skill Requirements. Defines multi-skill requirements.
  • Disposal of Nonconforming Products. Sets out disposal of nonconforming products.
  • Operation Control Plan. The plan controlling operations.
  • Quality Plan - Incoming Inspection and Testing. The quality plan for incoming inspection and testing.
  • Material Specifications. Specifies materials.
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 9001:2015 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
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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 10 real pages from the ISO 9001:2015 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 9001:2015 toolkit, frequently asked

Who is ISO 9001 for?+
ISO 9001:2015 is the world's most widely used quality management standard. It applies to any organisation of any size or sector that wants to deliver consistent quality, satisfy customers and win work that requires certification, from manufacturers and trading companies to service providers.
Does the kit show the process approach?+
Yes. It includes eight process flow charts covering customer service, marketing, purchasing, production, stores, quality control, engineering and research and development, so your quality system is documented as connected processes.
Does it cover design and development (clause 8.3)?+
Yes. There are R&D request and plan forms, a design verification report, design review report and minutes, a design and development monitoring register and an experiment data sheet, so you can apply clause 8.3 where it is relevant.
Is internal audit and management review included?+
Yes. You get an internal audit procedure with an audit plan, checklist and report, plus a management review agenda and minutes and a corrective action report, so you can run the full check-and-act cycle.
What format do I get?+
Everything is editable Microsoft Word. You replace the placeholders, including the company name, logo and scope, with your own details, then implement the procedures and record evidence on the formats.
What does the ISO 9001:2015 toolkit include?+
A clause-by-clause ISO 9001:2015 manual, 13 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 9001:2015 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 9001:2015 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 9001:2015 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

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ISO 9001:2015 Documentation Toolkit 79 documents, Word and Excel, delivery within 24 working hours $149