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Testing and Calibration Laboratories Β· ISO/IEC 17025:2017

ISO/IEC 17025:2017 Documentation Toolkit

The real ISO/IEC 17025:2017 documentation set we deliver: a complete management system for a testing or calibration laboratory, in 57 editable Word and Excel documents. It carries a clause-by-clause Quality Manual, 17 procedures and 39 forms, covering impartiality, measurement uncertainty and statistical evaluation, equipment control and calibration, handling of items, competence and the full management system, so you can build an accreditation-ready laboratory without hiring a consultant. Every document is listed and explained on this page.

57
Documents
in the kit
1
Quality manual
clause-by-clause
17
Procedures
clause-mapped
39
Forms and
records
$199
βœ“ Within 24h secure deliveryβœ“ Editable Word and Excelβœ“ Lifetime free updates
ISO/IEC 17025:2017MANUAL
Testing and Calibration Laboratories System Manual
Clause-by-clause structure
17Clause-mapped
procedures
39Ready-to-use
forms
Written to satisfy the requirements assessed by accreditation bodiesUKASANABA2LADAkkSILACIAF
Overview

Everything you need for ISO/IEC 17025:2017, in one download

Preparing the documentation is the slowest and most confusing part of getting certified to ISO/IEC 17025:2017. 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 17025:2017 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 testing and calibration laboratories 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

Built for a testing or calibration laboratory

A complete management system written to ISO/IEC 17025:2017, from impartiality and structure through the technical process requirements to the management system, so a lab can seek or maintain accreditation.

Measurement uncertainty and technical validity

A dedicated procedure for evaluating measurement uncertainty and the statistical evaluation of results, the technical core that distinguishes an accredited laboratory.

Equipment, calibration and traceability

Procedures and forms for equipment control, a calibration plan, a list of calibrated equipment and equipment log books, so measurements stay traceable and defensible.

Competent, authorized personnel

A skill matrix, competence gap assessment, authorization sheet and witness assessment, so you can evidence that the people who test and calibrate are competent and authorized.

Impartiality and confidentiality safeguarded

An impartiality management procedure, a threats-to-impartiality assessment, and a confidentiality and impartiality agreement, so you can demonstrate the independence an assessor checks.

Editable in Word and Excel

Every document is an editable Microsoft Word or Excel file, including the training plan, the witness assessment plan and the complaint and appeal register in Excel.

How the kit is built

Three tiers of documents that work together

Every kit follows the same proven structure, so it is easy to understand and easy to implement.

Tier 1

The Manual

The top level document. It answers ISO/IEC 17025:2017 clause by clause and sets out the scope of your system, your policy, the context of your organisation, and how your processes connect. This is the document an auditor opens first.

Tier 2

The Procedures

17 procedures that describe how you actually meet each requirement, from managing documents and training to internal audit and corrective action. They turn the manual into day-to-day practice.

Tier 3

The Forms and Records

39 ready-to-use forms and registers that capture the evidence an auditor wants to see. Sample filled forms are included so you can see exactly how each one is meant to be used.

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 17025:2017 Toolkit

A complete document set, fully editable in Microsoft Office.

Manual1
Procedures17
Forms and records39
Total files57

ISO/IEC 17025:2017 Laboratory Quality Management System Manual

The top-level document of the laboratory management system. Written to match ISO/IEC 17025:2017 clause by clause, it sets out the laboratory profile and authorization, the impartiality and confidentiality arrangements, the structure, and how each general, resource, process and management-system requirement is met. This is the document an assessor opens first.

Laboratory profile and authorization statementScope and references4. General requirements: impartiality and confidentiality5. Structural requirements6. Resource requirements: personnel, facilities, equipment, traceability7. Process requirements: sampling, testing, uncertainty, reporting8. Management system requirementsAnnexes: organization chart, document map, glossary
PROC Procedures (17)
  • Procedure for Context of the Organization. How the laboratory identifies the internal and external issues, interested parties and scope that shape the management system (Clause 4, 8.1).
  • Procedure for Environment Monitoring. How environmental conditions that affect test and calibration results are monitored and controlled (Clause 6.3).
  • Procedure for Evaluation of Measurement Uncertainty and Statistical Evaluation. How measurement uncertainty is estimated and results are evaluated statistically (Clause 7.6).
  • Procedure for Internal Audit. How internal audits of the management system are planned, conducted and reported (Clause 8.8).
  • Procedure for Communication. How internal and external communication is planned and recorded (Clause 8.1).
  • Procedure for Control of Records. How records are identified, stored, protected and retained (Clause 8.4).
  • Procedure for Corrective Action. How nonconformities are corrected and their causes addressed (Clause 8.7).
  • Procedure for Management of Changes. How changes to the management system are planned and controlled (Clause 8.5, 8.6).
  • Procedure for Management Review. How top management reviews the management system and sets actions (Clause 8.9).
  • Procedure for Control of Documents. How documented information is created, approved, issued, changed and retained (Clause 8.3).
  • Procedure for Customer Complaints and Appeal. How complaints and appeals are received, investigated and resolved (Clause 7.9).
  • Procedure for Training, Awareness and Competence. How competence is determined, training delivered and personnel authorized (Clause 6.2).
  • Procedure for Lab Operations. How test and calibration work is planned and carried out, from item handling to reporting of results (Clause 7).
  • Procedure for Purchasing and Sub-Contracting. How externally provided products and services are controlled and subcontracting managed (Clause 6.6).
  • Procedure for Master Equipment. How measuring and test equipment is registered, maintained and controlled (Clause 6.4).
  • Procedure for Handling of Calibration Items. How items for test or calibration are received, handled, protected and returned (Clause 7.4).
  • Procedure for Impartiality Management. How risks to impartiality are identified, assessed and managed, safeguarding valid results (Clause 4.1).
FORM Forms and records (39)
  • F-01 Management of Change Plan. Plans and controls a change to the management system.
  • F-02 Job Description. Defines the duties and competencies of a role.
  • F-03 Skill Matrix List. Maps personnel against the competencies each activity needs.
  • F-04 Competence Gap Assessment Checklist. Identifies gaps between required and actual competence.
  • F-05 List of Calibrated Equipment. The register of equipment and its calibration status.
  • F-06 Calibration Plan. Plans the calibration of measuring and test equipment.
  • F-07 Equipment Inspection Report (In-house). Records in-house inspection of equipment.
  • F-08 Approved Sub-contractor List. The controlled list of approved subcontractors.
  • F-09 Employee Training Report. Records training delivered to an employee.
  • F-10 Attendance Sheet. Records attendance at a training session.
  • F-11 Induction Training Report. Records induction training for new staff.
  • F-12 Employee Training Plan (Excel). Plans employee training across the year, in Excel.
  • F-13 Authorization Sheet. Authorizes personnel for specific test or calibration activities.
  • F-14 Technician Training and Assessment Process Form. Records the training and assessment of a technician.
  • F-15 Employee Training Record. Holds each employee training history.
  • F-16 Witness Assessment of Personnel, Site Activities Report. Records the witnessing of personnel performing activities.
  • F-17 Witness Assessment of Personnel, Site Activities Plan (Excel). Plans witness assessments of personnel, in Excel.
  • F-18 Equipment Log Book. Logs the use and status of an equipment item.
  • F-19 Supplier Registration Form. Registers a new supplier for evaluation.
  • F-20 Approved Vendor List. The controlled list of approved vendors.
  • F-21 Supplier Evaluation Form. Evaluates a supplier before approval.
  • F-22 Customer Feedback. Collects feedback from customers.
  • F-23 Complaint and Appeal Report. Records a complaint or appeal and its handling.
  • F-24 Complaint and Appeal Register (Excel). The register of all complaints and appeals, in Excel.
  • F-25 Document Change. Requests and records a change to a controlled document.
  • F-26 Minutes of Management Review Meeting. Records the management review decisions and actions.
  • F-27 List of Internal Auditors. The list of qualified internal auditors.
  • F-28 Internal Audit Schedule. Schedules the internal audits for the year.
  • F-29 Internal Audit NCR. Records a nonconformity raised at internal audit.
  • F-30 Corrective and Preventive Action Report. Records a corrective or preventive action from cause to verification.
  • F-31 Audit Checklist. The checklist used to conduct an internal audit.
  • F-32 Internal Audit Report. Reports the findings of an internal audit.
  • F-33 Terms and Conditions of the Laboratory Service. The terms and conditions that govern the laboratory service to a client.
  • F-34 Amendment and Change Record Form. Records amendments and changes to documents.
  • F-35 Sub-Contractor Evaluation Form. Evaluates a subcontractor before approval.
  • F-36 Non-Conformance Log. The log of all nonconformances.
  • F-37 SWOT Analysis Matrix. Records the strengths, weaknesses, opportunities and threats analysis.
  • F-38 Confidentiality and Impartiality Agreement. Captures each person confidentiality and impartiality commitment.
  • F-39 Identification and Assessment of Threats to Impartiality. Identifies and assesses threats to impartiality and the safeguards applied.
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/IEC 17025:2017 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

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/IEC 17025:2017 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 17025:2017 toolkit, frequently asked

Who is ISO/IEC 17025 for?+
ISO/IEC 17025:2017 sets the requirements for the competence, impartiality and consistent operation of testing and calibration laboratories. This toolkit gives a lab a complete management system to seek or maintain accreditation.
Does it cover measurement uncertainty?+
Yes. There is a dedicated procedure for the evaluation of measurement uncertainty and the statistical evaluation of results, which is central to ISO 17025 and closely examined at assessment.
How does it handle equipment and traceability?+
The kit includes procedures for equipment control and handling of calibration items, plus a calibration plan, a list of calibrated equipment and equipment log books, so your measurements stay traceable.
How does it handle impartiality?+
Impartiality is a general requirement of ISO 17025. The kit includes an impartiality management procedure, a form to identify and assess threats to impartiality, and a confidentiality and impartiality agreement.
Is ISO/IEC 17025:2017 the current edition?+
Yes. ISO/IEC 17025:2017 is the current edition for testing and calibration laboratories, and this toolkit is written to it.
What does the ISO/IEC 17025:2017 toolkit include?+
A clause-by-clause ISO/IEC 17025:2017 manual, 17 procedures, and 39 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 17025:2017 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 17025:2017 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 17025:2017 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 17025:2017 Documentation Toolkit 57 documents, Word and Excel, delivery within 24 working hours $199