QMS Non Conformities
1. Corrective Action Register
2. Design and Development
3. Non Conformance Register
4. Non Conformance Report
5. Non-Conformities And Corrective Actions Management
6. Action Register
7. Control Of Non-Conforming Products And Services
8. Corrective Action Checklist
QMS Policy And Manual
9. Organization Chart
10. Quality Management Plan
11. Quality Management System Manual
QMS Production And Service Provision
12. Inspection And Test Plan Log
13. Inspection And Test Records
14. Load Test Report
15. Post-Delivery Activities Checklist
16. Product Inspection And Testing Plan
17. Product Release Authorization
18. Product Release Certificate
19. Production And Service Provision
20. Production Check
21. Production Service Change Review Record
22. Quality Inspection Checklist
QMS Purchasing Procedure
23. Evaluation Supplier Checklist
24. Procurement Policy
25. Purchase Order Form
26. Supplier And Vendor Register
27. Supplier Change Order
28. Supplier Complaint Form
29. Supplier Pre-Qualification Form
30. Supplier Selection Criteria
31. Suppliers Registry Of Complaints
32. Vendor And Supplier Service Review
33. Vendor Pre-Qualification Form
34. Vendor Risk Assessment
QMS Risk And Opportunities
35. Risk Management Procedure
36. Risk Register
QMS Change Management
37. Change Control Form
38. Change Management Form
39. Change Management Procedure
40. Change Management Process Checklist
41. Change Request Log
QMS Customer Satisfaction
42. Customer Communication Plan
43. Customer Complaint Register
44. Customer Satisfaction Questionnaire
45. Customer Satisfaction Report
46. Customer Satisfaction Procedure
QMS Design And Development
47. Design and Development
48. New Product Design and Development Procedure
49. QMS Requirements Process
QMS Document Control
50. Document Control Procedure
51. Document Control Register
QMS Equipment Maintenance
52. Equipment Calibration And Maintenance Plan
53. Equipment Calibration Form
54. Equipment Maintenance Plan
QMS Human Resource
55. Human Resource Management Procedure
56. Organizational Knowledge Procedure
57. Training Program
58. Training Record And Attendance Register.1
59. Training Record Sheet
QMS Internal Audit
60. Internal Audit Checklist Excel
61. Internal Audit Checklist Word
62. Internal Audit Plan
63. Internal Audit Procedure
64. Internal Audit Report
65. Internal Audit Schedule
66. Internal Audit Status Report
67. ISO Internal Audit Dashboard
QMS Management Review
68. Excel Implementation plan-9001
69. Management Review Meeting Agenda PPT
70. Management Review Process
71. Project Plan ISO 9001
QMS Mandatory Documents
72. Corrective Action Request
73. Management Review Meeting
74. NCR CAR Register
75. Objectives And Targets
76. Quality Policy
77. Release Of Products And Services
78. Supplier Management Procedure
79. Training And Competency
ISO 9001 - Add-On Templates
80. Resource, Competence and Awareness Procedure-ISO 9001
81. Roles And Responsibility Matrix-ISO 9001
82. Root Cause Analysis Excel Template-ISO 9001
83. Sales Procedure-ISO 9001
84. Training Evaluation Format-ISO 9001
85. Training Needs Identification and Training Calendar-ISO 9001
86. Training Record and Attendance Register-ISO 9001
87. Vendor Selection and Evaluation Procedure-ISO 9001
88. Breakdown Analysis Format-ISO 9001
89. Calibration Equipment Tracker-ISO 9001
90. Change Management Form-ISO 9001
91. Context of the Organization and Interested Parties-ISO 9001
92. Context, Risk and Opportunity Procedure-ISO 9001
93. Contractor Management and Outsourcing Procedure-ISO 9001
94. Customer Satisfaction Procedure-ISO 9001
95. Document Control Procedure-ISO 9001
96. Excel Implementation plan-9001
97. Internal Audit Programme Schedule-ISO 9001
98. List of Internal Auditors-ISO 9001
99. Machine Breakdown Analysis-ISO 9001
100. Management Review Meeting Minutes-ISO 9001
101. Management Review Process-ISO 9001
102. Master list of Equipment's-ISO 9001
103. Master List of Suppliers- IS0 9001
104. New Product Design and Development Procedure-IS0 9001
105. Non-Conformities And Corrective Actions Management-ISO 9001
106. Non-Conformity Report-ISO 9001
107. Procedure for Stores, Issuance and Logstics-IS0 9001
108. Purchase Order Form-IS0 9001
109. Purchase Requisition Format-IS0 9001
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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.