Editable ISO 9001:2015 templates for policies, procedures, records and internal audit preparation, delivered as clearly scoped digital files.
Complete ISO 9001:2015 kit: quality manual, 36 procedures, audit checklist, gap analysis, forms, registers, project plan and training decks.
These files follow ISO 9001:2015. ISO 9001:2026 was published on 16 September 2026; certificates to the previous edition remain valid until 30 September 2029. Transition guidance
The Excel tools calculate live, and every Word document is fully written and editable. Change the answers below to see how the audit checklist works, then flip through samples of what you will download.
Change an answer below and watch the score, chart and readiness update instantly. This is a simplified version of the Excel checklist, which scores every question automatically.
The full Excel checklist scores all 112 questions automatically, with charts, a root-cause chart and a readiness dashboard.
Sample pages showing the structure and writing style of the documents in this kit. Every file you download is listed in the purchase box above.
Section 8.5 — Production and service provision
The organization carries out production and service provision under controlled conditions. Controlled conditions include the availability of documented information defining the characteristics of the products and the results to be achieved, suitable monitoring and measuring resources, and the use of competent people.
Outputs are identified by suitable means throughout production and service provision, and their status with respect to monitoring and measurement requirements is identified. Where traceability is a requirement, the organization controls the unique identification of outputs and retains the documented information needed to maintain traceability.
Planned arrangements are completed satisfactorily before release, and the release of products and services to the customer does not proceed until then, unless otherwise approved by a relevant authority. Documented information provides traceability to the person authorizing release.
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ISO 9001
Complete ISO 9001:2015 kit: quality manual, 36 procedures, audit checklist, gap analysis, forms, registers, project plan and training decks.
ISO 9001
Editable ISO 9001:2015 quality manual covering clauses 4–10, plus a QMS document map.
ISO 9001
32 editable ISO 9001:2015 procedures: 8 core QMS procedures plus 24 operational and support procedures.
Internal Audit
Audit programme, ISO 9001 audit checklist, corrective-action tracker and internal audit report template.
ISO 9001
Clause-by-clause ISO 9001:2015 audit checklist with conformance dashboard, plus a gap analysis workbook.
ISO 9001
Management review agenda, inputs, outputs and action log template, with management review guidance.
75 editable files · 55 Word · 16 Excel · 4 PowerPoint, grouped below into 22 areas. Everything is delivered instantly as editable Microsoft Office files with a cover page, headers, footers and styles ready to make your own, and is organised around ISO 9001:2015.
The documents are written in clear, professional language and follow the clause structure of ISO 9001:2015, so your certification body can quickly verify compliance without lengthy explanations.
The Complete Document Kit is our most comprehensive offering. It contains a fully written quality manual, 36 procedures covering everything from document control and internal auditing to corrective action and management review, plus forms, registers, checklists, process maps and training decks: 75 editable files in total. Together, these documents form a complete Quality Management System that you can customise with your organisation's name, logo, and specific process details.
The Quality Manual Template provides a top-level overview of your QMS. It includes sections on organisational context, quality policy, scope and exclusions, process interactions, and clause-by-clause compliance narratives. It is typically the first document an auditor will request, and our template ensures you make a strong first impression.
All templates are delivered as editable Microsoft Office files (Word, Excel and, in the complete kit, PowerPoint). After downloading, you should review each document and replace the placeholder text with information specific to your organisation. Pay particular attention to your scope statement, quality policy, organisational chart, and any process descriptions that need to reflect your actual workflows. Most organisations can complete the customisation process within two to four weeks, depending on the complexity of their operations.
If you are starting from scratch, we recommend beginning with the gap analysis checklist to understand which documents and processes you already have in place. From there, work through the quality manual, followed by your mandatory procedures, and finally the supporting forms and templates. This top-down approach ensures consistency across your entire QMS documentation suite.
Absolutely. Our templates are designed to work for organisations at any stage of their ISO 9001 journey, including those starting from scratch. Each document includes guidance notes and placeholder text that explain what information to add and why. We recommend beginning with the gap analysis checklist to understand your current position, then working through the quality manual and procedures in a logical order.
All templates are delivered as editable Microsoft Office files: Word (.docx) and Excel (.xlsx), plus PowerPoint (.pptx) training decks in the complete kit. You can open them in Microsoft Office, Google Docs, LibreOffice, or any compatible application. Every section is fully editable, so you can add your organisation's name, logo, and specific process details. There are no locked fields or password-protected sections. Once you download the files, they are yours to customise and use without any ongoing subscription or licence fees.
No template can guarantee certification. The files provide an ISO 9001:2015-aligned structure, but you must customise them to reflect your actual processes, operate the management system and retain objective evidence. Your certification body will make its own independent conformity decision.
