0 Browse kits
Home › Documentation Kits › ISO 9001:2026
Quality Management · ISO 9001:2026

ISO 9001:2026 Documentation Toolkit

The real ISO 9001:2026 documentation set: 367 documents that form a complete quality management system (QMS), written to the new sixth edition published in September 2026. The Quality Manual answers every clause of ISO 9001:2026, and you get 7 policies, 33 procedures, 21 work instructions, 146 forms each with a completed worked example, and 11 Excel tools, covering context and climate change, leadership, quality culture and ethical behaviour, risks and opportunities, planning of change, operation, design, purchasing, production, release, internal audit, management review and improvement, all editable in Word and Excel, so a company can build a certification-ready quality system without hiring a consultant.

367
Documents
and tools
33
Procedures
clause-mapped
146
Forms with
filled samples
11
Validated
Excel tools
$149
✓ Within 24h secure delivery✓ Editable Word and Excel✓ Lifetime free updates
ISO 9001:2026MANUAL
Quality Management System Manual
Clause-by-clause structure
33Clause-mapped
procedures
146Ready-to-use
forms
Written to satisfy the requirements checked byBSISGSTÜVBureau VeritasDNVIntertek
Overview

Everything you need for ISO 9001:2026, in one download

Preparing the documentation is the slowest and most confusing part of getting certified to ISO 9001:2026. 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 9001:2026 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

Written to the new ISO 9001:2026 edition

Every document is written to ISO 9001:2026, the sixth edition published in September 2026 that replaces ISO 9001:2015. You certify against the standard as it stands today, and you are ready for transition audits now.

Quality culture and ethical behaviour, covered

A dedicated policy, a leadership and quality culture procedure, a quality culture and engagement survey, leadership gemba walk records and an ethics and integrity concern report, so the new 2026 expectations on culture and ethics are evidenced, not just stated.

Risks and opportunities, handled separately

Separate procedures, registers and effectiveness reviews for risk and for opportunity, plus a planning-of-change procedure with impact assessment, implementation plan and change register, the areas the 2026 edition sharpened most.

Real tools, not just templates

11 working Excel tools, including SPC and process capability, Gauge R&R by ANOVA, AQL sampling to ISO 2859-1, a customer satisfaction and NPS analyser, a KPI dashboard and a cost of poor quality calculator.

Operations covered end to end

Procedures and work instructions for contract review, design and development, supplier control and audit, production, first article approval, special process validation, error-proofing, traceability, release and nonconforming output.

A completed example for every form

All 146 forms come with a matching sample filled form, worked around a realistic engineering company, so you can see exactly how each record should look before you complete your own.

How the set is structured

367 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.

MAN1Quality Manual
POL7Policies
QP33Procedures
WI21Work instructions
QF146Forms and registers
SMP146Sample filled forms
TOOL11Validated Excel tools
CUST2Customization pack
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 9001:2026 Toolkit

A complete document set, fully editable in Microsoft Office.

Quality Manual1
Policies7
Procedures33
Work instructions21
Forms and registers146
Sample filled forms146
Validated Excel tools11
Customization pack2
Total documents367

MAN-01 Quality Manual

The top-level description of the quality management system of the organisation. It traces each requirement to the procedure, work instruction, form, tool and record that satisfies it. This is the document an auditor opens first.

General and document controlIntroduction and organisation overviewScope, normative references, terms and definitions4. Context of the organisation, including climate change5. Leadership, quality culture and ethical behaviour6. Planning: risks, opportunities, objectives and change7. Support8. Operation9. Performance evaluation10. Improvement
POL Policies (7)
  • POL-01 Quality Policy. The statement of top management's intentions and commitments for quality at the organisation.
  • POL-02 Quality Culture and Ethical Behaviour Policy. Top management's commitments on the shared values, attitudes and behaviours that make quality work at the organisation, and on honest, ethical conduct in every decision that touches the customer.
  • POL-03 Risk and Opportunity Management Policy. Top management's commitments on how the organisation determines, evaluates and acts on risks and opportunities that can affect product conformity, delivery and customer satisfaction, including disruption.
  • POL-04 Customer Focus and Satisfaction Policy. Top management's commitments on understanding customer requirements, communicating with customers, handling feedback and complaints, and measuring and improving satisfaction at the organisation.
  • POL-05 External Provider Supplier Policy. Top management's commitments on how the organisation selects, controls, monitors and develops the external providers of processes, products and services that affect the quality of what we deliver.
  • POL-06 People Competence and Work Environment Policy. Top management's commitments on providing enough competent and aware people, developing their skills, and maintaining a physical, social and psychological work environment that supports conforming products at the organisation.
  • POL-07 Information Data Protection and Technology Use Policy. Top management's commitments on protecting documented information, customer and external provider information including personal data and intellectual property, and on the reliable use of technology that supports the quality management system at the organisation.
QP Procedures (33)
  • QP-01 Control of Documented Information. How the organisation creates, approves, issues, protects, changes, retains and disposes of the documents and records of its quality management system, including documents of external origin.
  • QP-02 Context of the Organization Interested Parties and QMS Scope. How the organisation determines and monitors the external and internal issues that affect its quality management system, including whether climate change is relevant, identifies relevant interested parties and their requirements, and sets and maintains the scope of the QMS.
  • QP-03 Process Management and Process Approach. How the organisation determines the processes of its quality management system, defines their inputs, outputs, sequence, interaction, criteria, resources, responsibilities and indicators, evaluates them and changes them in a controlled way.
  • QP-04 Leadership Roles Responsibilities and Quality Culture. How top management of the organisation demonstrates leadership and commitment to the quality management system and to customer focus, assigns and communicates roles, responsibilities and authorities, and builds and measures quality culture and ethical behaviour.
  • QP-05 Risk Management. How the organisation determines, analyses, evaluates and treats the risks that could stop it from consistently providing conforming products and services and enhancing customer satisfaction, including risks of disruption, and how it checks that its actions work.
  • QP-06 Opportunity Management. How the organisation identifies, evaluates and pursues opportunities that can improve its ability to consistently provide conforming products and services and to enhance customer satisfaction, and how it checks that the actions delivered the intended benefit.
  • QP-07 Quality Objectives and Planning to Achieve Them. How the organisation sets measurable quality objectives at company, function and process level, plans what will be done to achieve them, monitors and communicates progress, and updates them when needed.
  • QP-08 Planning and Control of Changes. How the organisation plans, approves, implements and reviews changes to its quality management system so that intended results are achieved and the integrity of the system is maintained at all times, including during the change.
  • QP-09 Legal Regulatory and Customer Requirements Identification. How the organisation identifies, records, communicates and keeps up to date the statutory and regulatory requirements that apply to its products, services and quality management system, and how it evaluates that they are met.
  • QP-10 Resource Planning Recruitment and Induction. How the organisation determines and provides the resources and the people needed for its quality management system and processes, recruits new employees and contract workers, and inducts every person before they start work.
  • QP-11 Competence Training and Awareness. How the organisation defines the competence needed for work that affects the quality management system, makes sure people are competent, closes gaps through training, mentoring, supervised work, re-assignment, hiring or contracting, checks that the action worked, and keeps everyone aware of the policy, objectives, their contribution, the consequences of nonconformity and the expected quality culture.
  • QP-12 Infrastructure and Maintenance. How the organisation determines, provides and maintains the buildings, utilities, production equipment, hardware and software, transport and information and communication technology needed to operate its processes and achieve conforming products and services.
  • QP-13 Environment for the Operation of Processes. How the organisation determines, provides and maintains the physical, social and psychological conditions needed to operate its processes and achieve conforming products and services, including laboratory conditions, the summer heat-stress programme, workload and wellbeing, and housekeeping.
  • QP-14 Control of Monitoring and Measuring Resources. How the organisation selects, identifies, calibrates or verifies, protects and controls the measuring equipment and other monitoring resources used to verify product and service conformity, and how it acts when equipment is found unfit.
  • QP-15 Organizational Knowledge Management. How the organisation works out which knowledge it needs to run its processes and reach the intended results of its QMS, keeps it, uses it and shares it, captures lessons learned, protects against the loss of knowledge when people leave, and acquires new knowledge when needs and trends change.
  • QP-16 Internal and External Communication. How the organisation decides what it communicates about its quality management system, when, with whom, how and by whom, inside the organization and with customers, external providers, regulators, the certification body and other interested parties, and how communications are recorded and checked for effect.
  • QP-17 Customer Communication Enquiry and Contract Review. How the organisation communicates with customers, defines the requirements for the products and services it offers, handles enquiries and quotations, reviews every order before accepting it, confirms requirements that are not in writing, and controls changes to orders.
  • QP-18 Design and Development of Products and Services. How the organisation plans, controls and records the design and development of custom skids, frames, fixtures and engineering changes for which it holds design responsibility, from inputs through reviews, verification, validation and release, to the control of design changes.
  • QP-19 Control of Externally Provided Processes Products and Services. How the organisation evaluates, selects, approves, monitors and re-evaluates external providers, decides the type and extent of control for each purchase, makes its requirements clear before sending them, and verifies what it receives, including outsourced processes such as galvanising, heat treatment, radiography and calibration.
  • QP-20 Control of Production and Service Provision. How the organisation plans and releases jobs, carries out machining, fabrication, welding, assembly and testing under controlled conditions, validates special processes, prevents human error, and reviews and controls changes to production, so that every part leaving a work centre conforms.
  • QP-21 Identification and Traceability. How the organisation identifies material, parts and assemblies from receipt to delivery, shows their inspection status at every stage, gives unique identities to items that must be traceable, and keeps the records that let any delivered item be traced back to its material and forward to every item made from the same heat.
  • QP-22 Property Belonging to Customers or External Providers. How the organisation takes care of property that belongs to customers or external providers while it is in our hands or being used by us: free-issue material and components, items sent for repair, gauges and tooling, drawings and models, premises where we work, returnable packaging and cylinders, and personal data.
  • QP-23 Preservation Storage Packaging and Delivery. How the organisation keeps material, work in progress and finished products in conforming condition from receipt to delivery: identification, handling, contamination control, storage, shelf-life control, packaging, transport and protection.
  • QP-24 Post Delivery Activities and Warranty. How the organisation decides what support each product family needs after delivery, and how it handles warranty claims, field service, installation support, spare parts and documentation, refurbishment, and end-of-life advice, so that customers get what was promised after the product leaves our gate.
  • QP-25 Inspection Testing and Release of Products and Services. How the organisation plans inspection and test points for every product, carries out final inspection and testing, checks the documentation pack, authorises release, issues the certificate of conformity, and controls the rare cases where a product is released before all planned verification is complete.
  • QP-26 Control of Nonconforming Outputs. How the organisation identifies, segregates and records outputs that do not meet requirements, decides what to do with them and who may decide, verifies corrected items again, informs customers when they are affected, and analyses nonconformities so that the costly ones lead to corrective action.
  • QP-27 Monitoring Measurement Analysis and Evaluation. How the organisation decides what to monitor and measure, how and when, how it makes sure the data is valid, and how it analyses and evaluates the results each month and each quarter to judge product conformity, customer satisfaction, QMS performance, the effect of plans and actions, external providers and the need for improvement.
  • QP-28 Customer Satisfaction and Complaints Handling. How the organisation obtains, monitors and reviews information on how satisfied its customers are, through surveys, meetings, scorecards, compliments, complaints and warranty claims, and how it receives, investigates, answers and learns from every complaint.
  • QP-29 Internal Audit. How the organisation plans its internal audit programme by risk, selects objective and impartial auditors, plans and conducts each audit, grades and reports findings to the managers concerned, and makes sure that correction and corrective action follow without undue delay.
  • QP-30 Management Review. How top management of the organisation reviews the quality management system twice a year and when events require it: how the inputs are prepared and analysed, how the review is run, what it must decide, how its conclusions on suitability, adequacy, effectiveness and strategic alignment are reached, and how actions are followed to completion.
  • QP-31 Nonconformity and Corrective Action. How the organisation reacts to every nonconformity, decides when and how deeply the cause must be investigated, finds root causes and similar risks elsewhere, takes actions in proportion to the effects, updates risks and the QMS, and proves that the actions worked before closing them.
  • QP-32 Continual Improvement. How the organisation finds, chooses, runs and verifies improvements to its processes, products, services and QMS: from employee suggestions handled in days to structured improvement projects, and how top management promotes improvement.
  • QP-33 Business Continuity and Disruption Response. How the organisation identifies the activities its customers depend on, plans how to keep providing conforming products and services during and after a disruption, responds when a disruption happens, keeps customers informed of contingency actions, and tests and improves its arrangements.
WI Work instructions (21)
  • WI-01-01 Document Numbering Formatting and Approval. Step-by-step instructions for numbering, formatting, reviewing and approving controlled documents of the organisation on the QMS document portal, so that every document is identified and approved the same way.
  • WI-01-02 Electronic Records Backup Access Control and Restoration. Step-by-step instructions for the IT Officer on backing up QMS data, controlling access rights and testing restoration, so that documented information stays available, protected and unaltered.
  • WI-02-01 PESTLE and SWOT Analysis Method. How to run the PESTLE analysis of external issues and the SWOT analysis of internal issues at the annual context workshop of the organisation, including the climate change questions, and how to record the results.
  • WI-05-01 Process Risk Analysis Using PFMEA. Step-by-step instructions for carrying out a process failure mode and effects analysis (PFMEA) on a machining, fabrication or assembly process at the organisation, and for transferring the results to the Risk Register.
  • WI-11-01 Operator Skills Qualification and Sign off. Step-by-step instructions for assessing and signing off a CNC operator or programmer as independent (competence level 2) on a machine type at the organisation, and for re-qualifying them.
  • WI-12-01 Preventive Maintenance of CNC Machining Centres. Step-by-step instructions for the daily, weekly, monthly, quarterly and annual preventive maintenance of CNC machining and turning centres at the organisation, including the accuracy checks that confirm the machine can still hold drawing tolerances.
  • WI-14-01 In-house Verification of Callipers and Micrometers. Step-by-step instructions for verifying vernier, dial and digital callipers and external micrometers in the quality laboratory of the organisation against calibrated gauge blocks, and for deciding whether they remain fit for use.
  • WI-14-02 Measurement System Analysis Gauge R&R. Step-by-step instructions for planning, running and evaluating a gauge repeatability and reproducibility study by the ANOVA method at the organisation, so that measurement systems used on critical characteristics are shown to be fit for their tolerance.
  • WI-17-01 Quotation Preparation and Costing. Step-by-step instructions for preparing, costing, checking and issuing a quotation at the organisation, so that every price rests on a correct reading of the requirements, a realistic routing and a delivery date the shop can meet.
  • WI-18-01 Design Verification and Validation Testing. Step-by-step instructions for the independent checking of design calculations and drawings and for the proof load and trial-fit tests used to verify and validate frames, lifting items and fixtures designed by the organisation, and for confirming that the test results support the acceptance criteria stated in the design outputs.
  • WI-19-01 Supplier Audit and Evaluation. Step-by-step instructions for planning, carrying out, scoring and reporting an audit of an external provider at the organisation, with emphasis on providers of outsourced special processes such as heat treatment, galvanising, painting and NDT.
  • WI-19-02 Incoming Inspection Sampling AQL. Step-by-step instructions for receiving inspection of externally provided products at the organisation: certificate review, sampling by attributes to ISO 2859-1, 100% checks of critical characteristics, and the accept or reject decision.
  • WI-20-01 Machine Set-up and First Article Approval. Step-by-step instructions for setting up a CNC machine or fabrication work station at the organisation and for inspecting and approving the first article before a batch runs.
  • WI-20-02 Validation of Welding as a Special Process. Step-by-step instructions for validating and revalidating welding at the organisation: qualifying welding procedures, qualifying welders and keeping their continuity, validating welding equipment, and monitoring parameters during production.
  • WI-20-03 Error-Proofing Poka-Yoke Design and Verification. Step-by-step instructions for choosing, designing, proving and checking error-proofing devices on production steps at the organisation, so that human errors are prevented or detected before parts leave the work station.
  • WI-23-01 Packaging Labelling and Dispatch. Step-by-step instructions for cleaning, preserving, packing, labelling and dispatching released products at the organisation, using three packaging levels and the customer's own packing specification where it is stricter.
  • WI-25-01 Final Inspection and Release. Step-by-step instructions for the QC Inspector and Yard QC Inspector to carry out final inspection against the ITP, record results, check the traceability record and documentation pack, and sign release within their authority.
  • WI-27-01 Statistical Process Control and Capability Analysis. Step-by-step instructions for setting up and using control charts on critical characteristics, reacting to out-of-control signals, and calculating process capability with tool T-07 at the organisation.
  • WI-28-01 Customer Satisfaction Survey Administration. Step-by-step instructions for preparing, sending, following up, entering and calculating the annual customer satisfaction survey and the post-project survey at the organisation, including the customer satisfaction index and the net promoter score.
  • WI-29-01 Conducting Audit Interviews and Sampling Evidence. Practical instructions for internal auditors at the organisation on how to interview people at their workplace, observe work, draw fair samples of records and record evidence that will stand up when it is checked.
  • WI-31-01 Root Cause Analysis Using 5 Whys and Fishbone. Step-by-step instructions for corrective action teams at the organisation on how to define a problem, list possible causes on a fishbone diagram, follow the likely ones with 5 Whys, prove the root cause with evidence, and check where else it could act.
QF Forms and registers (146)
  • QF-01-01 Master List of Documents. Lists every controlled internal document of the QMS with its current revision.
  • QF-01-02 Document Change Request. The controlled document change request form, used under QP-01 Control of Documented Information.
  • QF-01-03 Document Distribution and Withdrawal Record. Evidences the document distribution and withdrawal, used under QP-01 Control of Documented Information.
  • QF-01-04 Master List of Records and Retention Schedule. Lists every type of record retained by the QMS, where it is kept, who is responsible and the minimum retention period.
  • QF-01-05 External Documents Register. Keeps the external documents register up to date in one controlled place, used under QP-01 Control of Documented Information.
  • QF-01-06 Records Disposal Record. Evidences the records disposal, used under QP-01 Control of Documented Information.
  • QF-02-01 Internal and External Issues Register. Keeps the internal and external issues register up to date in one controlled place, used under QP-02 Context of the Organization Interested Parties and QMS Scope.
  • QF-02-02 Interested Parties Needs and Expectations Register. Keeps the interested parties needs and expectations register up to date in one controlled place, used under QP-02 Context of the Organization Interested Parties and QMS Scope.
  • QF-02-03 QMS Scope and Applicability Determination. Records the qms scope and applicability determination, used under QP-02 Context of the Organization Interested Parties and QMS Scope.
  • QF-02-04 Climate Change Relevance Assessment. Captures and reports the climate change relevance assessment, used under QP-02 Context of the Organization Interested Parties and QMS Scope.
  • QF-03-01 Process Definition Sheet Turtle Diagram. Records the process definition sheet turtle diagram, used under QP-03 Process Management and Process Approach.
  • QF-03-02 Process Interaction Matrix. Keeps the process interaction matrix up to date in one controlled place, used under QP-03 Process Management and Process Approach.
  • QF-03-03 Process Performance Evaluation Record. Evidences the process performance evaluation, used under QP-03 Process Management and Process Approach.
  • QF-04-01 Roles Responsibilities and Authorities Matrix. Keeps the roles responsibilities and authorities matrix up to date in one controlled place, used under QP-04 Leadership Roles Responsibilities and Quality Culture.
  • QF-04-02 Job Description. The controlled job description form, used under QP-04 Leadership Roles Responsibilities and Quality Culture.
  • QF-04-03 Quality Culture and Engagement Survey. Captures and reports the quality culture and engagement survey, used under QP-04 Leadership Roles Responsibilities and Quality Culture.
  • QF-04-04 Leadership Gemba Walk Record. Evidences the leadership gemba walk, used under QP-04 Leadership Roles Responsibilities and Quality Culture.
  • QF-04-05 Ethics and Integrity Concern Report. Captures and reports the ethics and integrity concern report, used under QP-04 Leadership Roles Responsibilities and Quality Culture.
  • QF-05-01 Risk Register. Keeps the risk register up to date in one controlled place, used under QP-05 Risk Management.
  • QF-05-02 Risk Treatment Plan. Plans and documents the risk treatment plan, used under QP-05 Risk Management.
  • QF-05-03 Risk Action Effectiveness Review. Captures and reports the risk action effectiveness review, used under QP-05 Risk Management.
  • QF-06-01 Opportunity Register. Keeps the opportunity register up to date in one controlled place, used under QP-06 Opportunity Management.
  • QF-06-02 Opportunity Evaluation and Business Case. Records the opportunity evaluation and business case, used under QP-06 Opportunity Management.
  • QF-06-03 Opportunity Action Effectiveness Review. Captures and reports the opportunity action effectiveness review, used under QP-06 Opportunity Management.
  • QF-07-01 Quality Objectives Register. Keeps the quality objectives register up to date in one controlled place, used under QP-07 Quality Objectives and Planning to Achieve Them.
  • QF-07-02 Objective Action Plan. Plans and documents the objective action plan, used under QP-07 Quality Objectives and Planning to Achieve Them.
  • QF-07-03 Objectives Progress Report. Captures and reports the objectives progress report, used under QP-07 Quality Objectives and Planning to Achieve Them.
  • QF-08-01 Change Request and Impact Assessment. Captures and reports the change request and impact assessment, used under QP-08 Planning and Control of Changes.
  • QF-08-02 Change Implementation Plan. Plans and documents the change implementation plan, used under QP-08 Planning and Control of Changes.
  • QF-08-03 Change Effectiveness Review. Captures and reports the change effectiveness review, used under QP-08 Planning and Control of Changes.
  • QF-08-04 Change Register. Keeps the change register up to date in one controlled place, used under QP-08 Planning and Control of Changes.
  • QF-09-01 Statutory and Regulatory Requirements Register. Keeps the statutory and regulatory requirements register up to date in one controlled place, used under QP-09 Legal Regulatory and Customer Requirements Identification.
  • QF-09-02 Compliance Evaluation Record. Evidences the compliance evaluation, used under QP-09 Legal Regulatory and Customer Requirements Identification.
  • QF-10-01 Resource Needs Assessment. Captures and reports the resource needs assessment, used under QP-10 Resource Planning Recruitment and Induction.
  • QF-10-02 Manpower Requisition. The controlled manpower requisition form, used under QP-10 Resource Planning Recruitment and Induction.
  • QF-10-03 Interview Evaluation Record. Evidences the interview evaluation, used under QP-10 Resource Planning Recruitment and Induction.
  • QF-10-04 Employee Induction Checklist. The employee induction checklist used to check and evidence conformity, used under QP-10 Resource Planning Recruitment and Induction.
  • QF-10-05 Personnel File Checklist. The personnel file checklist used to check and evidence conformity, used under QP-10 Resource Planning Recruitment and Induction.
  • QF-11-01 Training Needs Analysis. Captures and reports the training needs analysis, used under QP-11 Competence Training and Awareness.
  • QF-11-02 Annual Training Plan. Plans and documents the annual training plan, used under QP-11 Competence Training and Awareness.
  • QF-11-03 Training Attendance Sheet. Records the training attendance sheet, used under QP-11 Competence Training and Awareness.
  • QF-11-04 Training Feedback Form. The controlled training feedback form, used under QP-11 Competence Training and Awareness.
  • QF-11-05 Training Effectiveness Evaluation. Captures and reports the training effectiveness evaluation, used under QP-11 Competence Training and Awareness.
  • QF-11-06 Competence Matrix. Keeps the competence matrix up to date in one controlled place, used under QP-11 Competence Training and Awareness.
  • QF-11-07 Competence Evaluation Record. Evidences the competence evaluation, used under QP-11 Competence Training and Awareness.
  • QF-11-08 Awareness Briefing Record. Evidences the awareness briefing, used under QP-11 Competence Training and Awareness.
  • QF-12-01 Equipment and Infrastructure Register. Keeps the equipment and infrastructure register up to date in one controlled place, used under QP-12 Infrastructure and Maintenance.
  • QF-12-02 Preventive Maintenance Schedule. Keeps the preventive maintenance schedule up to date in one controlled place, used under QP-12 Infrastructure and Maintenance.
  • QF-12-03 Maintenance Work Order. The controlled maintenance work order form, used under QP-12 Infrastructure and Maintenance.
  • QF-12-04 Machine History Card. Keeps the machine history card up to date in one controlled place, used under QP-12 Infrastructure and Maintenance.
  • QF-12-05 IT Asset and Backup Log. Keeps the it asset and backup log up to date in one controlled place, used under QP-12 Infrastructure and Maintenance.
  • QF-13-01 Work Environment Assessment. Captures and reports the work environment assessment, used under QP-13 Environment for the Operation of Processes.
  • QF-13-02 Environmental Conditions Monitoring Log. Keeps the environmental conditions monitoring log up to date in one controlled place, used under QP-13 Environment for the Operation of Processes.
  • QF-13-03 Wellbeing and Workload Check-in. Records the wellbeing and workload check-in, used under QP-13 Environment for the Operation of Processes.
  • QF-13-04 5S Housekeeping Audit. The 5s housekeeping audit used to check and evidence conformity, used under QP-13 Environment for the Operation of Processes.
  • QF-14-01 Measuring Equipment Register. Keeps the measuring equipment register up to date in one controlled place, used under QP-14 Control of Monitoring and Measuring Resources.
  • QF-14-02 Calibration Schedule. Keeps the calibration schedule up to date in one controlled place, used under QP-14 Control of Monitoring and Measuring Resources.
  • QF-14-03 In-house Calibration and Verification Record. Evidences the in-house calibration and verification, used under QP-14 Control of Monitoring and Measuring Resources.
  • QF-14-04 External Calibration Certificate Review. Captures and reports the external calibration certificate review, used under QP-14 Control of Monitoring and Measuring Resources.
  • QF-14-05 Out of Tolerance Impact Assessment. Captures and reports the out of tolerance impact assessment, used under QP-14 Control of Monitoring and Measuring Resources.
  • QF-14-06 Gauge Repeatability and Reproducibility Study. Captures and reports the gauge repeatability and reproducibility study, used under QP-14 Control of Monitoring and Measuring Resources.
  • QF-15-01 Organizational Knowledge Register. Keeps the organizational knowledge register up to date in one controlled place, used under QP-15 Organizational Knowledge Management.
  • QF-15-02 Lessons Learned Record. Evidences the lessons learned, used under QP-15 Organizational Knowledge Management.
  • QF-15-03 Knowledge Transfer and Handover Plan. Plans and documents the knowledge transfer and handover plan, used under QP-15 Organizational Knowledge Management.
  • QF-16-01 Communication Matrix. Keeps the communication matrix up to date in one controlled place, used under QP-16 Internal and External Communication.
  • QF-16-02 Meeting Minutes. Records the meeting minutes, used under QP-16 Internal and External Communication.
  • QF-16-03 External Communication Log. Keeps the external communication log up to date in one controlled place, used under QP-16 Internal and External Communication.
  • QF-17-01 Customer Enquiry Register. Keeps the customer enquiry register up to date in one controlled place, used under QP-17 Customer Communication Enquiry and Contract Review.
  • QF-17-02 Contract and Order Review Checklist. The contract and order review checklist used to check and evidence conformity, used under QP-17 Customer Communication Enquiry and Contract Review.
  • QF-17-03 Quotation. The controlled quotation form, used under QP-17 Customer Communication Enquiry and Contract Review.
  • QF-17-04 Order Amendment Record. Evidences the order amendment, used under QP-17 Customer Communication Enquiry and Contract Review.
  • QF-17-05 Customer Requirement Confirmation. Records the customer requirement confirmation, used under QP-17 Customer Communication Enquiry and Contract Review.
  • QF-18-01 Design and Development Plan. Plans and documents the design and development plan, used under QP-18 Design and Development of Products and Services.
  • QF-18-02 Design Input Record. Evidences the design input, used under QP-18 Design and Development of Products and Services.
  • QF-18-03 Design Review Record. Evidences the design review, used under QP-18 Design and Development of Products and Services.
  • QF-18-04 Design Verification Record. Evidences the design verification, used under QP-18 Design and Development of Products and Services.
  • QF-18-05 Design Validation Record. Evidences the design validation, used under QP-18 Design and Development of Products and Services.
  • QF-18-06 Design Output Approval and Release. Records the design output approval and release, used under QP-18 Design and Development of Products and Services.
  • QF-18-07 Design Change Request. The controlled design change request form, used under QP-18 Design and Development of Products and Services.
  • QF-19-01 Supplier Pre-qualification Questionnaire. The controlled supplier pre-qualification questionnaire form, used under QP-19 Control of Externally Provided Processes Products and Services.
  • QF-19-02 Supplier Evaluation and Selection. Records the supplier evaluation and selection, used under QP-19 Control of Externally Provided Processes Products and Services.
  • QF-19-03 Approved Supplier List. Keeps the approved supplier list up to date in one controlled place, used under QP-19 Control of Externally Provided Processes Products and Services.
  • QF-19-04 Purchase Requisition. The controlled purchase requisition form, used under QP-19 Control of Externally Provided Processes Products and Services.
  • QF-19-05 Purchase Order Requirements Checklist. The purchase order requirements checklist used to check and evidence conformity, used under QP-19 Control of Externally Provided Processes Products and Services.
  • QF-19-06 Supplier Performance Scorecard. Records the supplier performance scorecard, used under QP-19 Control of Externally Provided Processes Products and Services.
  • QF-19-07 Supplier Audit Report. Captures and reports the supplier audit report, used under QP-19 Control of Externally Provided Processes Products and Services.
  • QF-19-08 Incoming Inspection Report. Captures and reports the incoming inspection report, used under QP-19 Control of Externally Provided Processes Products and Services.
  • QF-19-09 Supplier Corrective Action Request. The controlled supplier corrective action request form, used under QP-19 Control of Externally Provided Processes Products and Services.
  • QF-20-01 Production Plan and Schedule. Keeps the production plan and schedule up to date in one controlled place, used under QP-20 Control of Production and Service Provision.
  • QF-20-02 Job Card and Route Traveller. The controlled job card and route traveller form, used under QP-20 Control of Production and Service Provision.
  • QF-20-03 First Article Inspection Report. Captures and reports the first article inspection report, used under QP-20 Control of Production and Service Provision.
  • QF-20-04 In-process Inspection Record. Evidences the in-process inspection, used under QP-20 Control of Production and Service Provision.
  • QF-20-05 Special Process Validation Record. Evidences the special process validation, used under QP-20 Control of Production and Service Provision.
  • QF-20-06 Production Change Control Record. Evidences the production change control, used under QP-20 Control of Production and Service Provision.
  • QF-20-07 Error-Proofing Verification Checklist. The error-proofing verification checklist used to check and evidence conformity, used under QP-20 Control of Production and Service Provision.
  • QF-21-01 Traceability Register. Keeps the traceability register up to date in one controlled place, used under QP-21 Identification and Traceability.
  • QF-21-02 Inspection Status Tag Log. Keeps the inspection status tag log up to date in one controlled place, used under QP-21 Identification and Traceability.
  • QF-21-03 Traceability Exercise Record. Evidences the traceability exercise, used under QP-21 Identification and Traceability.
  • QF-22-01 Customer and External Provider Property Register. Keeps the customer and external provider property register up to date in one controlled place, used under QP-22 Property Belonging to Customers or External Providers.
  • QF-22-02 Property Loss or Damage Report. Captures and reports the property loss or damage report, used under QP-22 Property Belonging to Customers or External Providers.
  • QF-23-01 Stores Receipt and Issue Record. Evidences the stores receipt and issue, used under QP-23 Preservation Storage Packaging and Delivery.
  • QF-23-02 Storage Condition Inspection. Records the storage condition inspection, used under QP-23 Preservation Storage Packaging and Delivery.
  • QF-23-03 Packing and Dispatch Checklist. The packing and dispatch checklist used to check and evidence conformity, used under QP-23 Preservation Storage Packaging and Delivery.
  • QF-23-04 FIFO and Shelf-life Control Log. Keeps the fifo and shelf-life control log up to date in one controlled place, used under QP-23 Preservation Storage Packaging and Delivery.
  • QF-24-01 Post-delivery Requirements Assessment. Captures and reports the post-delivery requirements assessment, used under QP-24 Post Delivery Activities and Warranty.
  • QF-24-02 Warranty Claim Register. Keeps the warranty claim register up to date in one controlled place, used under QP-24 Post Delivery Activities and Warranty.
  • QF-24-03 Field Service Report. Captures and reports the field service report, used under QP-24 Post Delivery Activities and Warranty.
  • QF-25-01 Inspection and Test Plan. Plans and documents the inspection and test plan, used under QP-25 Inspection Testing and Release of Products and Services.
  • QF-25-02 Final Inspection Report. Captures and reports the final inspection report, used under QP-25 Inspection Testing and Release of Products and Services.
  • QF-25-03 Certificate of Conformity. Records the certificate of conformity, used under QP-25 Inspection Testing and Release of Products and Services.
  • QF-25-04 Release Authorization Record. Evidences the release authorization, used under QP-25 Inspection Testing and Release of Products and Services.
  • QF-26-01 Nonconforming Output Report. Captures and reports the nonconforming output report, used under QP-26 Control of Nonconforming Outputs.
  • QF-26-02 Nonconforming Output Log. Keeps the nonconforming output log up to date in one controlled place, used under QP-26 Control of Nonconforming Outputs.
  • QF-26-03 Concession Request. The controlled concession request form, used under QP-26 Control of Nonconforming Outputs.
  • QF-26-04 Rework and Repair Verification Record. Evidences the rework and repair verification, used under QP-26 Control of Nonconforming Outputs.
  • QF-27-01 Monitoring and Measurement Plan. Plans and documents the monitoring and measurement plan, used under QP-27 Monitoring Measurement Analysis and Evaluation.
  • QF-27-02 Monthly Quality Performance Report. Captures and reports the monthly quality performance report, used under QP-27 Monitoring Measurement Analysis and Evaluation.
  • QF-27-03 Data Analysis and Evaluation Report. Captures and reports the data analysis and evaluation report, used under QP-27 Monitoring Measurement Analysis and Evaluation.
  • QF-28-01 Customer Satisfaction Survey. Captures and reports the customer satisfaction survey, used under QP-28 Customer Satisfaction and Complaints Handling.
  • QF-28-02 Customer Satisfaction Analysis. Captures and reports the customer satisfaction analysis, used under QP-28 Customer Satisfaction and Complaints Handling.
  • QF-28-03 Customer Complaint Form. The controlled customer complaint form, used under QP-28 Customer Satisfaction and Complaints Handling.
  • QF-28-04 Customer Complaint Register. Keeps the customer complaint register up to date in one controlled place, used under QP-28 Customer Satisfaction and Complaints Handling.
  • QF-28-05 Customer Feedback and Compliments Log. Keeps the customer feedback and compliments log up to date in one controlled place, used under QP-28 Customer Satisfaction and Complaints Handling.
  • QF-29-01 Annual Internal Audit Programme. Plans and documents the annual internal audit programme, used under QP-29 Internal Audit.
  • QF-29-02 Internal Audit Plan. Plans and documents the internal audit plan, used under QP-29 Internal Audit.
  • QF-29-03 Internal Audit Checklist. The internal audit checklist used to check and evidence conformity, used under QP-29 Internal Audit.
  • QF-29-04 Internal Audit Report. Captures and reports the internal audit report, used under QP-29 Internal Audit.
  • QF-29-05 Audit Finding Report. Captures and reports the audit finding report, used under QP-29 Internal Audit.
  • QF-29-06 Auditor Competence and Impartiality Record. Evidences the auditor competence and impartiality, used under QP-29 Internal Audit.
  • QF-29-07 Audit Programme Review. Captures and reports the audit programme review, used under QP-29 Internal Audit.
  • QF-30-01 Management Review Agenda. Plans and documents the management review agenda, used under QP-30 Management Review.
  • QF-30-02 Management Review Input Pack. Records the management review input pack, used under QP-30 Management Review.
  • QF-30-03 Management Review Minutes. Records the management review minutes, used under QP-30 Management Review.
  • QF-30-04 Management Review Action Log. Keeps the management review action log up to date in one controlled place, used under QP-30 Management Review.
  • QF-31-01 Nonconformity and Corrective Action Report. Captures and reports the nonconformity and corrective action report, used under QP-31 Nonconformity and Corrective Action.
  • QF-31-02 Corrective Action Register. Keeps the corrective action register up to date in one controlled place, used under QP-31 Nonconformity and Corrective Action.
  • QF-31-03 Root Cause Analysis Worksheet. Captures and reports the root cause analysis worksheet, used under QP-31 Nonconformity and Corrective Action.
  • QF-31-04 Corrective Action Effectiveness Verification. Records the corrective action effectiveness verification, used under QP-31 Nonconformity and Corrective Action.
  • QF-32-01 Improvement Suggestion Form. The controlled improvement suggestion form, used under QP-32 Continual Improvement.
  • QF-32-02 Improvement Project Charter. Plans and documents the improvement project charter, used under QP-32 Continual Improvement.
  • QF-32-03 Improvement Register. Keeps the improvement register up to date in one controlled place, used under QP-32 Continual Improvement.
  • QF-33-01 Business Impact Analysis. Captures and reports the business impact analysis, used under QP-33 Business Continuity and Disruption Response.
  • QF-33-02 Contingency Plan. Plans and documents the contingency plan, used under QP-33 Business Continuity and Disruption Response.
  • QF-33-03 Disruption Incident Log. Keeps the disruption incident log up to date in one controlled place, used under QP-33 Business Continuity and Disruption Response.
  • QF-33-04 Contingency Exercise Record. Evidences the contingency exercise, used under QP-33 Business Continuity and Disruption Response.
  • QF-33-05 Customer Contingency Notification. The controlled customer contingency notification form, used under QP-33 Business Continuity and Disruption Response.
Every form above is also provided as a completed sample filled form, worked around a realistic organisation. That is 146 additional worked examples included in the set.
TOOL Validated Excel tools (11)
  • T-01 Risk and Opportunity Assessment Calculator. Scores risks and opportunities on likelihood and consequence and ranks the actions.
  • T-02 Quality Objectives and KPI Dashboard. Tracks quality objectives and KPIs against target with a live dashboard.
  • T-03 Supplier Evaluation and Performance Scorecard. Evaluates, scores and ranks suppliers on quality, delivery and service.
  • T-04 Customer Satisfaction Index and NPS Analyser. Calculates the customer satisfaction index and Net Promoter Score from survey data.
  • T-05 Calibration Schedule and Test Uncertainty Ratio Tracker. Schedules calibration and tracks the test uncertainty ratio of each instrument.
  • T-06 Gauge R&R Calculator ANOVA method. Runs a Gauge R&R study by the ANOVA method and judges measurement system capability.
  • T-07 SPC Control Chart and Process Capability. Plots SPC control charts and calculates process capability (Cp, Cpk).
  • T-08 AQL Sampling Plan Selector ISO 2859-1. Selects sampling plans and acceptance numbers to ISO 2859-1 AQL tables.
  • T-09 Risk-based Internal Audit Programme Planner. Builds a risk-based internal audit programme across processes and the year.
  • T-10 Competence Gap and Training Effectiveness Analyser. Maps competence gaps and evaluates training effectiveness by role.
  • T-11 Cost of Poor Quality Calculator. Calculates the cost of poor quality across prevention, appraisal and failure.
CUST Customization pack (2)
  • PKG-01 Customization Guide. How to turn the toolkit into your organisation's own controlled documents: what to decide, what to replace, how to tailor the tools and how to keep the set current.
  • PKG-01A Register, Cross-reference Matrix and Placeholder Guide. A cross-reference of every document to the ISO 9001:2026 clauses and a guide to every placeholder you replace.
What you gain

Why teams choose a ready-made kit

✓
Save months of work

The writing is done. You edit instead of authoring from a blank page.

✓
Avoid consultant fees

Get a professional system for a fraction of the cost of hiring one.

✓
Nothing missed

Mapped clause by clause so every requirement is covered.

✓
Written in plain English

Easy to read, easy to adapt, no jargon you have to decode.

✓
Audit-ready evidence

Forms and registers capture exactly what an auditor asks to see.

✓
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 9001:2026 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

📥

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.

👥

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

★★★★★

The documents were well structured and easy to adapt. We cleared our certification audit with no major findings.

Quality ManagerManufacturing, United Kingdom
★★★★★

Saved us weeks of writing. Everything was mapped to the clauses, so we knew nothing was missing.

Operations LeadFood business, UAE
★★★★★

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 9001:2026 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 9001:2026 toolkit, frequently asked

Is this the new ISO 9001:2026 edition?+
Yes. The whole set is written to ISO 9001:2026, the sixth edition published in September 2026, which replaces ISO 9001:2015. Certified organisations have a three-year transition period, and this kit gives you a system written to the new text from day one.
What changed in ISO 9001:2026, and does the kit cover it?+
The 2026 edition strengthens leadership expectations on quality culture and ethical behaviour, separates risks and opportunities more clearly, and sharpens planning of change. The kit has dedicated policies, procedures, forms and tools for each of these.
Who is ISO 9001 for?+
ISO 9001 is the world's most widely used quality management standard. It applies to any organisation of any size or sector that wants consistent quality, satisfied customers and the certification many tenders and customers require.
Does every form come with a filled example?+
Yes. All 146 forms are provided both blank and as a completed sample filled form, worked around a realistic organisation.
What formats do I get?+
Everything is editable Microsoft Word and Excel, including the 11 Excel tools. You replace the [Company Name] and other placeholders with your own details, guided by the customization pack.
What does the ISO 9001:2026 toolkit include?+
A clause-by-clause ISO 9001:2026 manual, 33 procedures, and 146 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 9001:2026 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 9001:2026 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 9001:2026 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

14001
ISO 14001:2026
Environmental Management
136 documents$149
45001
ISO 45001:2018
Occupational Health & Safety
154 documents$149
27001
ISO 27001:2022
Information Security
120 documents$149
42001
ISO/IEC 42001:2023
AI Management Systems
138 documents$149

Get your ISO 9001:2026 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 9001:2026 Documentation Toolkit $149