Overview of T1 
Quality System Document Pack
This module presents model quality system documents which contain a sample Quality Manual as well as numerous quality procedures and forms. These are provided to give you a good start to developing your company's ISO 9001:2000 quality management system. In using them you must consider that:

  • you will need to amend them to suit the needs of your business;

  • some of them may not be appropriate for your business and should be ignored;

  • you will almost certainly need to define additional operational procedures to ensure that you comply with the requirements of ISO 9001:2000;

  • the style and layout are for guidance only and you can convert them to any style that is appropriate to your business.

These materials also include assessment questionnaires, guides and flowcharts which can be used by company personnel to help them plan, develop and implement their quality management system in their organisation.
Content
Quality Manual  
QM - Quality Manual  
 
Quality Procedures
QP 01 - Control of Non Conformance
QP 02 - Control of Quality Records
QP 03 - Corrective and Preventive Action
QP 04 - Document Change Control
QP 05 - Internal Auditing  
 
Operational Processes
OP 01 - Calibration of Measuring Equipment
OP 02 - Internal Communication
OP 03 - Computer Back - Up
OP 04 - Control of External Documents
OP 05 - Customer Focus
OP 06 - Design Control
OP 07 - Stock Control
OP 08 - Stock Inspections
OP 09 - Inspection of Incoming Material
OP 10 - Training
OP 11 - Inspection of Product
OP 12 - Job Descriptions
OP 13 -Maintenance of Plant and Equipment
OP 14 - Order Review
OP 15 - Preservation of Product
OP 16 - Performance Reporting
OP 17 - Plant Infrastructure & Work Environment
OP 18 - Supplier Assessment and Approval
OP 19 - Planning Product Realisation
OP 20 - Purchase Order Processing
OP 21 - Quality Management Review
OP 22 - Review of Quality Objectives
OP 23 - Quality Planning
OP 24 - Application of Statistical Techniques  
 
Flowcharts
Administration
Document Control
Design Process
Goods Receiving Process
Order Review
Quality Planning  
 
Useful Guides
Cost of Quality and Case Studies
Infrastructure and Environment
Internal Communications
ISO 9001 Structures
Lost Profit & Case Studies
Performance Reporting
Quality Objectives
Quality Policy
Requirements for procedures & records
Statistical Techniques  
 
Plans
Calibration Schedule
ISO 9001:2000 Project Plan
ISO 9001: Documentation
Product Realisation Plan
Internal Audits Plan
Equipment Maintenance Schedule
Management Review Agenda
Production Meeting Agenda
Sales Review Meeting Agenda
Staff Training Plan and Matrix
Quality Plan
 
Questionnaires
Customer Satisfaction Questionnaire
ISO 9001 Assessment  Questionnaire
Supplier Assessment Questionnaire
 
Records
Calibration - Test Record
Training - Staff Record
Suppliers - Approved List
Quality Records - Register
Stock Control - Inspection Form
Audits - Internal Audit Report
Audits - Internal Audit Checklist
Corrective Action - Register
Corrective Action - Form
Purchasing - Order Form
Document Control - Master Register for Controlled Documents
Document Control - Master Register for External Documents
Document Control - Change Note Register for Controlled Documents
Document Control - Change Note Form for Controlled Documents
Management Review - Meeting Minutes
 
General
End User Licence Agreement
User guide - Navigational aids
FAQs - Frequently Asked Questions