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ISO 9001 Policies Procedures Manual
Based on ISO 9001:2008
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Weight: 5 pounds
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Procedures Manual Sections:
ISO 9001 Quality Procedures
Over 440 pages of prewritten materials in a three ring binder organized by colored tabs. You will also receive a CD with all content in editable Microsoft® Word files for easy customization. Works with Microsoft Word 2003 and above.
Table of Contents
Document Control Procedure
- Document Distribution
- Document Revision
- Procedure and Work Instruction Format
- Temporary Changes
- Request For Document Change (RDC)
- Document Change Control
Quality Records Procedure
- Identification of Quality Records
- Record Generation
- Record Maintenance
- Quality Records
Management Responsibility Procedure
- Planning
- Management Representative
- Responsibilities and Authorities
- Management Review
Job Descriptions Procedure
- Preparation
- Format and Content
- Job Description Format
Competence, Awareness and Training
- New employee selection
- New Employee Orientation
Quotation Process Procedure
- Standard Products
- Custom or modified products and services
Sales Orders Procedure
- Sales Representatives
- Customer Service
- Credit Department
- Internet Orders
- Changes to orders.
Customer Complaints Procedure
- General
- Receiving a Contact/ customer Complaint
- Trouble Shooting/Problem Diagnosis
- Repairs and/or Replacements
- Trend Analysis
- Customer Service Log
- Customer Service Contact Form
Returned Goods Aithorization Procedure
- Origination
- Receiving Goods and Processing
- Returned Goods Authorization
Warranty and Service Policies Procedrue
- Warranty Coverage
- Service Programs
- Parts Pricing
- Limited Warranty
Design and Development Procedure
- New Product Initiation
- Design and Development Inputs
- Design Planning
- Product Development
- Design and Development Output
- Design Review and Verification
- Design Validation
- Design Completion Checklist For Electromechanical Devices
- Design Completion Checklist For Non-Electromechanical Devices
- Request For Engineering Action (REA)
Design Change Procedure
- Request for Design and/or Process Changes
- Engineering Change Notice
- Engineering Change Notice (ECN)
Pre-Production Quality and Planning
- Design Completion
- Design Transfer and Documentation
- Production Plan
- Product Design Release Form
Supplier Evaluation Procedure
- Vendor classification
- Vendor evaluation
- Vendor Files
- New Vendor Notification
- Vendor Survey Form
Purchasing Procedure
- Order Determination and Requisition
- Order Placement
- Record keeping and Matching
- Purchase Requisition
- Purchase Order
- Purchase Order Log
- Purchase Order Follow-Up
Receiving and Inspection
- Receiving
- Inspection
- Stocking
- Rejection, Discrepancies and Disposition
- Receiving Log
- Receiving And Inspection Report
- Production Planning
- Work Order Packets
Manufacturing Procedure
- Kitting Work Orders
- Production
- Final Inspection.
- Packaging and Labeling
- Final Release
Part Number Assignment Procedure
- Number Designation
- Part Number Assignment/Record Keeping
- Classification System
Serial Number Designation Procedure
- Serial Numbering
Product Labeling Procedure
- Label Control
- Identification Labels
- Safety Hazard Labels
Customer Property Procedure
- Receipt, Inspection and Stocking of Customer Supplied Items
- Unsuitable or Missing Items
- Customer Supplied Tooling and Fixtures
- Intellectual Property
- Material Return Notice
Control of Monitoring and Measuring Devices Procedure
- General requirements
- Storage, Handling and Maintenance
- Calibration System
- Inspection of Special Tooling
- Out-of-tolerance Conditions
- Control of Subcontractor Calibration
- Test Software
- Calibration Record
Customer Satisfaction Procedure
- General
- Post-Sale Follow-Up
- Customer Survey
- Post-Service Follow-Up
- Post Sale Satisfaction Report
- Customer Satisfaction Survey
- Customer Satisfaction Report
Internal Quality Audits Procedure
- Audit Guide
- Audit Process
- Corrective Action
- Audit Records
- Quality Assurance Audit Checklist
Monitoring and Measurement of Processes Procedure
- Effectiveness Criteria
- Reporting
- Improvement
- Review
Control of Nonconforming Product Procedure
- Identification and Segregation
- Nonconformance Report
- Returned Goods
- Disposition
- Corrective Action
- Nonconformance Report
Data Analysis and Continual Improvement Procedure
- Data collection
- Data analysis
- Continual Improvement
Corrective Action
- Initiating a Corrective Action
- Investigating the Cause
- Taking Corrective Action
- Preventing Recurrence
- Verification and Closure
- Corrective Action Request
Preventive Action Procedure
- Product Design
- Process Design
- Preventive Actions from Data Analysis
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