Quality Management System Templates

An ISO 9001 Quality Manual containing over 50 sections covering all the requirements of the ISO 9001 Standard.

  • Saving You 1000's of Hours Writing Your Own Documents.
  • Fully compliant with the ISO 9001:2008 certification standard and contains a comprehensive set of procedure templates covering all the clauses of the standard.
  • Record templates covering all the compulsory requirements of the new ISO 9001 certification standard, plus a set of optional supplementary records.

Download Samples:

QMS 1 Quality Management System

ISO 9001 2008 Changes and Compliance Summary

QMR 008 Register of Customer Property

QMR 016 Complaint Investigation Form

ISO 9001:2008 Quality Manual Guide:

  • Clearly matches our documents and procedures to the clauses of the ISO 9001:2008 standard. This is invaluable in ensuring you achieve ISO 9001 certification.

'With You All the Way' Step by Step Guide for Implementation of our ISO 9001 Quality Manual Package:

  • We guide you through a logical and structured approach to implementing and integrating our procedures and records into your quality management system.

Below is a summary of the documents provided and how they match up with the clauses of the standard:

ISO 9001:2008 Section Document Number Policy / Procedure Title
Quality Management System
4.1 Introduction QM001 Quality Management System
4.2 Documentation QM002 QMS Manual Summary
4.2.3 Internal Document Control QM003 Document Control
4.2.3 External Document Control QM004 Customer, Statutory and Regulatory Conformance
4.2.4 Quality System Records QM005 Record Control
Management Responsibility
5.1 Management Commitment QM006 Management Commitment
5.2 Customer Focus QM007 Quality Policy
5.3 Quality Policy
5.4 Planning QM001 Quality Management System
5.5 Responsibility & Authority QM008 Responsibility and Authority
5.5 Internal Communication
5.6 Management Review QM009 Management Review
Resource Management
6.1 Resources QM010 Resources and Training
6.2 Human Resources & Training
6.3 Infrastructure QM011  Infrastructure and Work Environment
6.4 Work Environment
Product Realization
7.1 Planning QM012 Contract Review
7.2 Customer Related Processes
7.3 Design and Development QM013 Design and Development
7.4 Purchasing, Orders and Verification of Purchased Materials QM014 Purchasing, Orders and Verification of Purchased Materials
7.5 Operational Control QM015 Production
7.5.1 Production
7.5.2 Validation of Processes
7.5.3  Identification and Traceability QM016 Identification and Traceability
7.5.4 Customer Property QM017 Customer Property
7.5.5 Preservation of Product QM018 Preservation of Product
QM019 Dispatch and Distribution
QM020 Maintenance
QM021 Waste Management
7.6 Calibration QM022 Calibration
Measurement, Analysis and Improvement
8.1 General QM023 Measurement and Monitoring
8.2 Monitoring and Measurement
8.2.1 Customer Satisfaction QM024 Customer Satisfaction
8.2.2 Internal Audit QM025 Internal Audit
8.2.3 Monitoring and Measuring QMS Processes QM026 Monitoring and Measuring QMS, Analysis of Data
8.2.4 Monitor and Measure Product Characteristics QM023 Measurement and Monitoring
8.3 Control of Non-Conforming Product QM027 Control of Non-Conforming Product
8.4 Analysis of Data QM026 Monitoring and Measuring QMS, Analysis of Data
8.5 Corrective Action, Preventive Action and Improvement QM028 Corrective Action, Preventive Action and Improvement
QM029 Crisis Management
QM030 Product Recall


Quality Management System Record Templates

Included in the package are a set of record templates covering all the compulsory requirements of the new ISO 9001 certification standard. Records included in the package:

  • 1 Management Review Minutes
  • 2 Training Record
  • 3 Product Release Record
  • 4 Design and Development Records
  • 5 Supplier Assessment Record
  • 6 Validation Record
  • 7 Identification and Traceability Record
  • 8 Register of Customer Property
  • 9 Calibration Record
  • 10 Internal Audit Record
  • 11 Records of Non-conforming Product
  • 12 Corrective Action Request Form
  • 13 Preventative Action Request Form
  • 14 Supplier Self Assessment and Approval Form

Plus we provide a set of optional supplementary records.

By Carl Barton - Managing Partner. (Google+)

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