Everything a small or medium-sized business (up to 100 employees) needs to build an ISO 9001:2015-compliant quality management system from scratch. The pack has been created by experienced ISO consultants and contains 49 documents across two file types: Word procedures and forms, and Excel registers and trackers.
The templates include helpful guidance throughout, making it quicker and easier for you to create your own QMS management system, tailored to your business.
Quality Management Document Templates: Quality Management Manual, Quality Policy, Organisational Chart, Context of the Organisation, Checklist Management System Change.
Procedure Templates: Document Control Procedure, Management System Change Process, Management Review Procedure, Resource Management Procedure, Customer Processes Procedure, Purchasing Procedure, Service Provision and Operations, Internal Auditing Procedure, Monitoring, Measurement and Improvement, Objectives, Targets and Programmes, Risk Assessment Procedure, Control of Equipment Procedure, Design and Development Procedure, Job Description Template.
Forms and Register Templates: Master Document and Record List, Management System Change Form, Management Review Protocol, Competence Matrix, Induction Checklist, Training Matrix, Training Attendance List, Employee Performance Review, Quality Project Plan, Goods-In Inspection Record, Customer Satisfaction Survey, Risk and Opportunity Register, Approved Supplier List, Quality Report, Supplier Quality Questionnaire, Complaint Investigation Form, Maintenance Register, Audit Programme, Objectives, Targets and Programmes Register, Overall Risk and Opportunity Register, Nonconformance and Improvement Register, Continual Improvement Tracker, Equipment Calibration Register, Legislation Register, Audit Report, Customer Satisfaction Dashboard, Employee Satisfaction Survey, Employee Satisfaction Dashboard, Sales Quotation, Sales Tracker, Invoice Template.
Upon purchase, you will be provided with a .zip file containing all of the documents in one file.
What is Included
Getting Started Guide
34 Forms and Registers and Examples
13 QMS Procedures and Examples
Quality Management Manual Template
Quality Policy Template and Example
Document Cross-Reference Guide
£149.99
Includes all taxes
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Will completing this template pack guarantee certification?
No template pack can guarantee certification, and any that claims otherwise should be treated with scepticism. Certification is awarded by an independent certification body based on their assessment of how well your quality management system is implemented and embedded in your organisation - not on the basis of documentation alone.
What the pack does is give you a complete, professionally structured set of documents that satisfies all the documented information requirements of ISO 9001:2015. That removes one of the biggest barriers to certification for most SMEs. But auditors will also look at whether your people understand and follow the procedures, whether your records reflect real activity, and whether the QMS is genuinely improving performance over time. A completed template pack is a strong foundation - not a shortcut past the implementation work.
Will I need any other documentation?
The pack covers all the documented information explicitly required or commonly expected under ISO 9001:2015. For most general manufacturing and service businesses, the pack is comprehensive and requires no additions.
That said, two situations may require additional documentation beyond what is included. First, if your business operates in a regulated sector - medical devices, aerospace, food, or pharmaceuticals, for example - you may be subject to sector-specific requirements that go beyond ISO 9001:2015. The pack does not include sector-specific documentation. Second, if your processes are highly complex or unusual, your certification body may expect more detailed work instructions for critical operations than this pack provides. Work instructions are process-specific and cannot be templated in a meaningful way, so they are intentionally excluded - you will need to write those for your own processes.
Your certification body can advise on any additional documentation they expect to see before your Stage 1 audit.
Is the pack suitable for any business type?
The pack is designed for small and medium-sized businesses across manufacturing, engineering, and professional services, typically, for those with around 10-100 employees. Those with fewer than 10 employees are likely to find that they do not need the full pack presented here and might overcomplicate their management system. For those over 100 employees you may need more complex documentation. In this case we would recommend engaging the expertise of an ISO Consultant to support you on some or all of the work.
The templates we have provided are written to be sector-neutral, and the underlying procedures - document control, risk management, supplier management, internal auditing, corrective action - apply equally to service businesses.
There are two sectors where the pack may need supplementing. Businesses pursuing ISO 9001 certification alongside a sector-specific standard — such as IATF 16949 for automotive, AS9100 for aerospace, or ISO 13485 for medical devices - will need additional documentation to meet those standards' additional requirements. Businesses that do not carry out design and development activities can simply exclude QP13 from their QMS scope, as the standard explicitly allows this where design is not part of the organization's remit.
How long will it take to complete?
The honest answer is that it depends more on your organisation than on the templates. The documents themselves can be adapted relatively quickly - most SMEs find they can work through the full set in four to eight weeks of part-time effort, typically with one person taking the lead. The Quality Management Manual and the procedures require the most thought because they need to reflect how your business actually operates, not just what the standard requires.
The bigger time investment is implementation - getting people trained and aware, running your first management review, completing at least one full internal audit cycle, and building up a set of quality records that demonstrate the system is working. Certification bodies typically want to see at least three to six months of QMS operation before the Stage 2 certification audit, so the overall timeline from starting work to holding a certificate is usually six to twelve months for an SME approaching certification for the first time.
What format are the files in?
Procedures and forms are Word (.docx) files; registers, matrices, trackers, and dashboards are Excel (.xlsx) files. All files are fully editable with no locked fields or restrictions. You do not need any specialist software beyond Microsoft Word and Excel (or compatible alternatives such as Google Office).
Which certification bodies will accept these documents?
The documents are designed to satisfy the requirements of ISO 9001:2015 as assessed by any certification body accredited by a national accreditation body that is a member of the IAF (International Accreditation Forum). This includes UKAS-accredited bodies in the UK, ANAB- and IAS-accredited bodies in the US, and INAB-accredited bodies in Ireland. ISOCentral is independent and has no affiliation with any certification body.
Can I edit and rebrand the documents?
Yes. Once purchased, the documents are yours to edit, populate, and use within your organisation. You may adapt them freely to suit your processes and brand. You may not resell or redistribute the templates commercially.
Is there support available if I get stuck?
The template pack is designed to be self-sufficient - the blank templates include detailed guidance prompts, and the completed examples show you exactly how a completed document should look. ISOCentral also publishes free guidance articles covering all major areas of ISO 9001:2015 implementation. If you need hands-on support, our directory lists verified consultants across the UK, US, and Ireland who may be able to help.
What is the difference between this pack and hiring a consultant?
A consultant will typically charge £3,000–£10,000 ($5,000 - $15,000) or more to develop QMS documentation for a small business, and the documents they produce will be proprietary to their engagement. This pack gives you professionally structured documentation at a fraction of that cost, which you own outright.
The trade-off is that you are doing the implementation work yourself - the template pack gives you the structure and the model, but it does not replace the thinking and the embedding that makes a QMS real. Many businesses use both: they purchase the pack to have a solid documentation foundation and then engage a consultant for a smaller scoping or readiness review engagement.
There is no right or wrong answer - every business is different. If you want to get a quote to understand the likely costs, fill in our quote request form via the button at the top of this page.
How do I know when I am ready for an ISO 9001 certification audit?
A good rule of thumb is that you are ready when:
- your QMS has been operating for at least three months
- you have completed at least one full internal audit cycle with findings recorded and closed
- you have held at least one management review with documented outputs
- you have quality records (inspection records, training records, nonconformity records) that reflect real activity in your business.
The Document Cross-Reference Guide included in the pack lists all 49 documents and indicates which are typically reviewed at each stage of the certification process.
£149.99
Includes all taxes
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