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Validation & Verification Bodies Β· ISO/IEC 17029 + ISO 14065

ISO/IEC 17029 + ISO 14065 Documentation Toolkit

The real ISO/IEC 17029 and ISO 14065 integrated documentation set we deliver: a complete management system for a validation and verification body, in 78 editable documents and tools. It carries a Validation and Verification Manual, 18 procedures, 7 exhibits and policies, 3 standard operating procedures and 47 forms, covering impartiality, competence, the full validation and verification process from request to statement, appeals and complaints, and a clause-by-clause document matrix mapping both standards. It suits any-sector validation and verification bodies and greenhouse gas and environmental verification bodies, so you can build a system to ISO/IEC 17029 and ISO 14065 without hiring a consultant.

78
Documents
and tools
18
Procedures
clause-mapped
47
Forms and
formats
3
Field safety
SOPs
$199
βœ“ Within 24h secure deliveryβœ“ Editable Word and Excelβœ“ Lifetime free updates
ISO/IEC 17029 + ISO 14065MANUAL
Validation & Verification Bodies System Manual
Clause-by-clause structure
18Clause-mapped
procedures
47Ready-to-use
forms
Written to satisfy the requirements assessed by accreditation bodiesUKASANABA2LADAkkSILACIAF
Overview

Everything you need for ISO/IEC 17029 + ISO 14065, in one download

Preparing the documentation is the slowest and most confusing part of getting certified to ISO/IEC 17029 + ISO 14065. 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/IEC 17029 + ISO 14065 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 validation & verification bodies 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

Two standards, one validation and verification system

A single management system that satisfies ISO/IEC 17029 for validation and verification bodies in any sector and ISO 14065 for bodies validating and verifying environmental and greenhouse gas information, which is a sector application of ISO 17029.

The full validation and verification process

Procedures and forms for the request, planning, execution, review, decision and the validation or verification statement, so the whole engagement is controlled and evidenced.

Impartiality and competence, evidenced

An impartiality procedure and policy, impartiality check and agreement forms, and a competence framework with assessment, skill matrix and evaluator qualification, which accreditation bodies examine closely.

Ready for GHG and environmental verification

Because ISO 14065 builds on ISO/IEC 17029, the kit suits a body verifying greenhouse gas assertions and other environmental information, as well as validation and verification in any other sector.

Appeals, complaints and use of marks

Procedures and registers for appeals and complaints and a procedure for the correct use of the accreditation and body marks, all of which an assessor checks.

A clause-by-clause document matrix

A document matrix maps the system against both ISO/IEC 17029 and ISO 14065, so you can show a peer evaluator exactly where every requirement is met.

How the set is structured

78 controlled documents in 6 tiers

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

MAN1Validation and Verification Manual
QP18Procedures
E7Exhibits and policies
SOP3Standard operating procedures
F47Forms and formats
TOOL2Risk sheet and document matrix
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/IEC 17029 + ISO 14065 Toolkit

A complete document set, fully editable in Microsoft Office.

Validation and Verification Manual1
Procedures18
Exhibits and policies7
Standard operating procedures3
Forms and formats47
Risk sheet and document matrix2
Total documents78

ISO/IEC 17029 and ISO 14065 Validation and Verification Management System Manual

The top-level document of the validation and verification body. Written to ISO/IEC 17029:2019 and ISO 14065:2020, it sets out the principles and scope, the impartiality and structural arrangements, the competence framework and the validation and verification process, mapping the requirements of both standards. This is the document a peer evaluator opens first.

Principles and scope4. General requirements: impartiality, liability, confidentiality5. Structural requirements6. Resource requirements: personnel and competence7. Process: request, planning, execution, review, decision and statement8. Information requirements9. Management system requirementsAnnexes: documentation structure, competence, document matrix
QP Procedures (18)
  • QP/VMS/01 Impartiality. How risks to impartiality are identified, evaluated and managed to safeguard independent decisions.
  • QP/VMS/02 Operational Control. How the operations of the validation and verification body are planned and controlled.
  • QP/VMS/03 Personnel and Training. How personnel are recruited, trained and their records maintained.
  • QP/VMS/04 Managing Competence. How the competence of validators and verifiers is defined, assessed and maintained.
  • QP/VMS/05 Procurement of Externally Provided Products and Services. How externally provided products and services are procured and controlled.
  • QP/VMS/06 Review of Requests, Tenders and Contracts. How requests, tenders and contracts are reviewed before acceptance.
  • QP/VMS/07 Planning. How a validation or verification engagement is planned.
  • QP/VMS/08 Execution. How a validation or verification is carried out against the plan.
  • QP/VMS/09 Review and Reporting. How the results are reviewed and the validation or verification statement is issued.
  • QP/VMS/10 Receive, Evaluate and Make Decisions on Appeals. How appeals against decisions are received, evaluated and decided.
  • QP/VMS/11 Receive, Evaluate and Resolve Complaints. How complaints are received, evaluated and resolved.
  • QP/VMS/12 Use of Marks. How the accreditation symbol and body marks are controlled and used correctly.
  • QP/VMS/13 Management Review. How top management reviews the system and sets actions.
  • QP/VMS/14 Internal Audit. How internal audits are planned, conducted and reported.
  • QP/VMS/15 Control of Nonconformity. How nonconforming work is identified, controlled and corrected.
  • QP/VMS/16 Risk Assessment. How risks and opportunities to the body are assessed and treated.
  • QP/VMS/17 Document and Data Control. How documents and data are created, approved, issued and changed.
  • QP/VMS/18 Control of Records. How records are identified, stored, protected and retained.
E Exhibits and policies (7)
  • E/VMS/01 Principles and Scope of Accreditation. The principles and the scope of accreditation the body works to.
  • E/VMS/02 Documentation Structure. The structure of the management system documentation.
  • E/VMS/03 Impartiality Policy. The body commitment to impartial validation and verification.
  • E/VMS/04 Confidentiality Policy. How information obtained during work is kept confidential.
  • E/VMS/05 Operational Control Plan. The plan of operational controls across the process.
  • E/VMS/06 Competence Requirements. The competence requirements for validators and verifiers.
  • E/VMS/07 Calibration Periodicity. The calibration periodicity for measuring and monitoring equipment.
SOP Standard operating procedures (3)
  • SOP/VMS/01 Protection. How personnel and information are protected during engagements.
  • SOP/VMS/02 Site Safety. How safety is maintained during on-site validation and verification.
  • SOP/VMS/03 Evaluators Qualification. How evaluators are qualified for their assigned work.
F Forms and formats (47)
  • F/QP/VMS/01/01 Impartiality and Confidentiality Agreement. Captures each person impartiality and confidentiality commitment.
  • F/QP/VMS/01/02 Impartiality Check Report. Records the check of impartiality for an engagement.
  • F/QP/VMS/03/01 Training Calendar. The calendar of planned training.
  • F/QP/VMS/03/02 Training Report. Records training delivered.
  • F/QP/VMS/03/03 Induction Training Report. Records induction training.
  • F/QP/VMS/03/04 Job Description. Defines a role and its requirements.
  • F/QP/VMS/03/05 Skill Matrix. Maps personnel against required skills.
  • F/QP/VMS/03/06 Training Effectiveness Check Report. Evaluates whether training was effective.
  • F/QP/VMS/03/07 Interview Report. Records a recruitment or competence interview.
  • F/QP/VMS/04/01 Employees Competence Chart. Maps employee competence across activities.
  • F/QP/VMS/04/02 Competence Assessment Report. Records the assessment of competence.
  • F/QP/VMS/05/01 Purchase Order. Raises a purchase order.
  • F/QP/VMS/05/02 Indent. Records a material or service indent.
  • F/QP/VMS/05/03 Supplier Registration Form. Registers a new supplier.
  • F/QP/VMS/05/04 Approved Vendor List. The controlled list of approved vendors.
  • F/QP/VMS/05/05 Supplier Evaluation Report. Records the evaluation of a supplier.
  • F/QP/VMS/05/06 Inspection Report. Records inspection of received goods or services.
  • F/QP/VMS/05/07 Subcontractors Agreement. The agreement that binds a subcontractor.
  • F/QP/VMS/06/01 Validation Verification Request. Captures a client request for validation or verification.
  • F/QP/VMS/06/02 Planning Register. Registers planned validation and verification engagements.
  • F/QP/VMS/06/03 Client Feedback Form. Collects client feedback.
  • F/QP/VMS/06/04 Validation Verification Agreement. The agreement for a validation or verification engagement.
  • F/QP/VMS/07/01 Validation Verification Plan. The plan for a validation or verification engagement.
  • F/QP/VMS/08/01 Validation Verification Execution. Records the execution of a validation or verification.
  • F/QP/VMS/08/02 Calibration Status of Equipment. Tracks calibration status of equipment.
  • F/QP/VMS/08/03 Equipment History Card. Records the history of an equipment item.
  • F/QP/VMS/09/01 Validation Verification Review and Decision Report. Records the review and decision on an engagement.
  • F/QP/VMS/09/02 Validation Verification Statement. The validation or verification statement issued to the client.
  • F/QP/VMS/10/01 Appeal Report. Records an appeal and its handling.
  • F/QP/VMS/10/02 Appeal Register (Excel). The register of all appeals, in Excel.
  • F/QP/VMS/11/01 Complaint Report. Records a complaint and its handling.
  • F/QP/VMS/11/02 Complaint Register (Excel). The register of all complaints, in Excel.
  • F/QP/VMS/13/01 Quality Objectives. Records the quality objectives and their targets.
  • F/QP/VMS/13/02 Improvement Log. Logs improvement actions.
  • F/QP/VMS/13/03 Circular. Issues an internal circular.
  • F/QP/VMS/13/04 Minutes of Meeting. Records the minutes of a meeting.
  • F/QP/VMS/14/01 Audit Plan and Schedule. Plans and schedules internal audits.
  • F/QP/VMS/14/02 Internal Audit Nonconformity Report. Records a nonconformity raised at internal audit.
  • F/QP/VMS/14/03 Audit Checklist (Management Representative). The audit checklist for the management representative areas.
  • F/QP/VMS/14/04 Audit Checklist (Technical Manager). The audit checklist for the technical areas.
  • F/QP/VMS/15/01 Nonconformity Work Report. Records nonconforming work.
  • F/QP/VMS/15/02 Corrective Action Report. Records a corrective action from cause to verification.
  • F/QP/VMS/16/01 Risk Assessment and Opportunity Sheet (Excel). Scores risks and opportunities to the body, in Excel.
  • F/QP/VMS/17/01 Master List and Distribution List of Documents. Indexes and distributes controlled documents.
  • F/QP/VMS/17/02 Change Note. Requests and records a document change.
  • F/QP/VMS/17/03 Periodic Document Review Report. Records the periodic review of documents.
  • F/QP/VMS/18/01 Master List of Records. The master index of records.
TOOL Risk sheet and document matrix (2)
  • Risk Assessment and Opportunity Sheet (Excel). A working risk and opportunity assessment sheet for the body, in Excel.
  • Document Matrix, ISO/IEC 17029 and ISO 14065. Maps the system clause by clause against both ISO/IEC 17029 and ISO 14065.
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.

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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/IEC 17029 + ISO 14065 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$199 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

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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
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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/IEC 17029 + ISO 14065 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/IEC 17029 + ISO 14065 toolkit, frequently asked

What is the relationship between ISO/IEC 17029 and ISO 14065?+
ISO/IEC 17029:2019 sets the general requirements for validation and verification bodies in any sector. ISO 14065:2020 is a sector application of ISO/IEC 17029 for bodies validating and verifying environmental and greenhouse gas information, adding GHG-specific requirements. This kit runs both together.
Who is this kit for?+
It is for a validation and verification body, including a greenhouse gas or environmental verification body, that wants a management system built to ISO/IEC 17029 and ISO 14065 for accreditation.
Does it cover the whole validation and verification process?+
Yes. There are procedures and forms for the request, planning, execution, review, decision and the validation or verification statement, plus impartiality, competence, appeals, complaints and the use of marks.
Does it include a document matrix?+
Yes. A document matrix maps the system clause by clause against both ISO/IEC 17029 and ISO 14065, so you can trace every requirement to its evidence.
What formats do I get?+
Everything is editable Microsoft Word and Excel, including the appeal, complaint and risk registers in Excel. You replace the highlighted placeholders and the example organisation details with your own before use.
What does the ISO/IEC 17029 + ISO 14065 toolkit include?+
A clause-by-clause ISO/IEC 17029 + ISO 14065 manual, 18 procedures, and 47 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/IEC 17029 + ISO 14065 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/IEC 17029 + ISO 14065 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/IEC 17029 + ISO 14065 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/IEC 17029 + ISO 14065 Documentation Toolkit 78 documents, Word and Excel, delivery within 24 working hours $199