Change Management
1.Change Control Form
2.Change Management Form
3.Change Management Procedure
4.Change Management Process Checklist
5.Change Request Log
Customer Satisfaction
6.Customer communication plan
7.Customer Complaint Register
8.Customer Satisfaction Procedure
9.Customer Satisfaction Questionnaire
10.Customer Satisfaction Report
Design and Development
11.Design and Development Plan
12.New Product Design And Development Procedure
13.Requirement Process
Document Control
14.Document Control Procedure
15.Document Control Register
Equipment Maintenance
16.Equipment Calibration And Maintenance Plan
17.Equipment Calibration Form
18.Equipment Maintenance Plan
Human Resource
19.Human Resource Management Procedure
20.Organisational Knowledge Procedure
21.Training And Competency
22.Training Program
23.Training Record And Attendance Register
24.Training Record Sheet
Internal Audit
25.Internal Audit Checklist Excel
26.Internal Audit Checklist Word
27.Internal Audit Dashboard
28.Internal Audit Plan
29.Internal Audit Procedure
30.Internal Audit Report
31.Internal Audit Schedule
32.Internal Audit Status Report
33.Project Plan
Management Review
34.Excel Implementation plan
35.Management Review Meeting
36.Management Review Process
37.Minutes of Meeting Agenda PPT Template
Non Conformities
38.Action Register
39.Control Of Non-Conforming Products And Services
40.Corrective Action Checklist
41.Corrective Action Register
42.Corrective Action Request
43.NCR CAR Register
44.Non-Conformance Register
45.Non-Conformance Report
46 Nonconformities and corrective action management procedure
47.Nonconformities and Corrective Actions Management
Policy and Manual
48.Objectives And Targets
49.Organization Chart
50.Quality Management Plan
51.Quality Management System Manual
52.Quality Policy
Production and Service Provision
53.Inspection And Test Plan Log
54.Inspection And Test Records
55.Load Test Report
56.Post-delivery activities checklist
57.Product Inspection And Testing Plan
58.Product Release Authorization
59.Product Release Certificate
60.Production And Service Provision
61.Production Check
62.Production Service Change Review Record
63.Quality Inspection Checklist
64.Release Of Products And Services
Purchasing Procedure
65.Evaluation Supplier Checklist
66.Procurement Policy
67.Purchase Order Form
68 Supplier And Vendor Register
69.Supplier Change Order
70.Supplier Compliant Form
71.Supplier Management Procedure
72.Supplier Pre-Qualification Form
73.Supplier Selection Criteria
74.Supplier Service Review Form
75.Suppliers Registry Of Complaints
76.Vendor Pre-Qualification Form
77.Vendor Risk Assessment
Risk and Opportunities
78.Risk Management Procedure
79.Risk Register
Add-On Templates
80. Breakdown Analysis Format
81. Calibration Equipment Tracker
82. Change Management Form
83. Context of the Organization and Interested Parties
84. Context, Risk and Opportunity Procedure
85. Contractor Management and Outsourcing Procedure
86. Customer Satisfaction Procedure
87. Document Control Procedure
88. Excel Implementation Plan
89. Internal Audit Programme Schedule
90. List of Internal Auditors
91. Machine Breakdown Analysis
92. Management Review Meeting Minutes
93. Management Review Process
94. Master List of Equipment
95. Master List of Suppliers
96. New Product Design and Development Procedure
97. Non-Conformities And Corrective Actions Management
98. Non-Conformity Report
99. Procedure for Stores, Issuance and Logistics
100. Purchase Order Form
101. Purchase Requisition Format
102. Resource, Competence and Awareness Procedure
103. Roles And Responsibility Matrix
104. Root Cause Analysis Excel Template
105. Sales Procedure
106. Training Evaluation Format
107. Training Needs Identification and Training Calendar
108. Training Record and Attendance Register
109. Vendor Selection and Evaluation Procedure
Welcome to ISO Docs. Our priority at ISO Docs is to provide high-quality templates and help our customers be efficient. Our goal is to create quality templates so that our customers can avoid rework and focus on their actual jobs rather than doing everything from scratch. We have dedicated support ready to assist you in any way we can.
Your Complete DIY Blueprint to ISO 9001 Success. No consultant needed.
Included in the toolkit, the Implementation Plan is your blueprint for building a complete DIY Quality Management System (QMS). It lays out every step, action, and timeline required to achieve ISO 9001 compliance. Combined with 100+ professionally designed templates—covering everything from internal audits to document control—it gives you all the tools you need to implement, manage, and continuously improve your QMS with confidence.
All The Essential Tools for Quality Management
Lay the groundwork for a strong, ISO 9001-compliant Quality Management System. These templates help you define your quality objectives, document your QMS framework, and communicate your commitment to excellence across your organization. With ready-to-use documents like the Quality Policy, QMS Manual, Management Plan, and Organization Chart, you'll have everything you need to align teams, meet requirements, and drive continuous improvement from the top down.
Everything You Need for a Flawless Internal Audit
Stay audit-ready with a complete set of internal audit tools—professionally designed to meet ISO 9001 standards. From the Internal Audit Checklist (Excel & Word) and Audit Plan to the Internal Audit Report, Schedule, Status Dashboard, and List of Auditors, these templates cover every step of the audit process. Whether you're preparing, executing, or following up, this toolkit makes internal audits simple, structured, and fully compliant.
Run Effective, Compliant Management Reviews—Effortlessly
Our toolkit includes everything you need to plan, conduct, and document ISO 9001-compliant management reviews. With templates like the Management Review Meeting Minutes, Management Review Process, Agenda (PPT), and the Excel Implementation Plan, you can ensure structured, insightful meetings that drive improvement and meet audit expectations. Simplify your reviews, stay organized, and keep your leadership loop fully engaged.
Take Control of Every Non-Conformity and Drive Corrective Action with Confidence.
Easily identify, document, and resolve process issues with our complete set of templates for non-conformities and corrective actions. From NCR and CAR forms to root cause analysis templates and tracking registers, these tools help you respond effectively, eliminate recurring problems, and meet ISO 9001 clause 10.2 requirements with confidence.