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IATF 16949:2016 Quality Manual and Procedures

Save Time, Save Money, and Simplify Certification with the RIGHT QMS!

Starting at $397.00

Created in MS Word for easy editing

Easy to customize for your organization

The manual references related procedures

Building your QMS is a cornerstone of any successful IATF 16949 Registration. But why take the risk of starting from scratch? With our fully customizable Quality Manual and Procedures Package you will have all the processes and documents you need.

All you have to do is edit and customize each element to suit your own organization and needs. The Quality Manual and Procedures package is ideally suited for organizations and consultants in search of a proven, simple pathway to successful Registration.

As you implement your IATF 16949 system you will also need checklists and training. You can save time and money by purchasing our Certification Packages!

Profit from the years of work that have gone into creating and refining this package. The key to an effective Quality Management System is designing the Quality Management Processes for efficiency and ease of use. The processes must be carefully thought out, well-organized, and carefully designed to work together to lead your organization to continuous improvement.

We save you time and money in gaining IATF 16949 certification.

How long would it take you to create hundreds of pages, formatted to comply with IATF 16949? Just think about the labor savings alone!

Our experienced IATF 16949 professionals have done the hard part for you. Our system is the result of continual improvement of processes and procedures that have been tried, proven and improved over the last decade. They have lead thousands of companies across the globe to successful IATF 16949 Registration, and more importantly to internal improvements including increased productivity and profits that IATF 16949 training and implementation brings.

Every purchase is backed by our guarantee so there is little risk in trying.

  • Quality Manual in MS Word format for ease of editing
  • 28 Procedures are written in MS Word and are ready for your customization
  • 63 Related Forms are written in MS Word or Excel
  • Text to address each requirement of the IATF 16949 Standard
  • Very clear instructions in obvious Blue Text to show you where to customize your Manual and Procedures
  • Required references to the recommended procedures and forms for your quality management system
  • Intuitive architecture for easy Document Control
    • We’ve numbered the sections of the Quality Manual to correspond with the sections of the IATF 16949 Standard. Registrars LOVE this feature!
    • Procedure and Form numbers relate to the section in the Quality Manual.
  • This is a downloadable product.
    • You will also have the option of purchasing the files on a Jump-Drive during checkout but it is not necessary.
IATF 16949 Documentation Templates

  • Quality Manual meets the IATF requirements
  • All documents are written in MS Word or Excel format for ease of editing.
  • 29 Procedures describing QMS Processes,
  • 1 Work instruction,
  • 63 Forms referenced by the procedures
  • Included in the Quality Manual folder are:
  • Template-Instructions,
  • Matrix that reflects the ‘Documentation Flow-Down’ and a “QMS-Docs-List” that represents ALL the documented information you get in the QMS package.
  • Technical Support

16949-2016 QMS Documents, Procedures, and Forms Matrix

Procedures Forms
P-400 Organizational context F-440-001 QMS-Process identification worksheet
P-500 Leadership F-440-002 Organizational context worksheet
P-600 Planning for the Quality Management System F-440-003 Product safety worksheet
P-612 Preventive action F-610-001 Risk and opportunity worksheet
P-710 Resource management F-612-001 Contingency plans worksheet
P-715 Control of monitoring and measuring equipment F-620-001 Quality objectives planning record
P-720 Competence and awareness F-710-001 Equipment problem report
P-740 Communication F-710-002 Resource maintenance record
P-750 Control of documented information F-715-001 Equipment calibration list
P-810 Operational planning and control F-715-001 Laboratory requirements worksheet
P-820 Customer related processes F-720-001 Training action plan
P-830 Design and development of products F-720-002 Group training record
P-831 Design and development of manufacturing processes F-720-003 Job description
P-840 Control of external providers F-720-004 Employee training summary
P-851 Control of production F-720-005 Auditor competency worksheet
P-852 Identification and traceability F-740-001 Comment and suggestion report
P-854 Preservation F-750-001 List of documented information
P-857 Other operational control F-750-002 Records matrix
P-860 Release of products and services F-750-003 Master documentation lists
P-870 Control of nonconforming outputs F-750-004 Quality records table
P-910 Monitoring, measurement, analysis and evaluation F-750-005 Document change request form
P-911 Statistical techniques F-750-006 Document revision checklist
P-912 Customer satisfaction F-750-007 Software inventory spreadsheet
P-913 Root cause analysis F-810-002 Project planning worksheet
P-920 Internal audit F-820-001 Client assessment report
P-930 Management review F-820-002 Production order
P-1010 Improvement F-830-001 Design plan
P-1020 Nonconformity and corrective action F-830-002 Design review record
F-830-003 Design change form
F-840-001 Provider assessment report
F-840-002 List of acceptable sources
F-840-003 Provider corrective action request – PCAR
F-840-004 Purchase requisition
F-840-005 Purchase order
F-840-006 Business agreement – contract
F-851-001 Process routing sheet – summary
F-851-002 Process routing sheet – summary
F-851-003 Process validation worksheet
F-851-006 External property control log
F-851-010 Control plan worksheet
F-852-001 Identification tag
F-852-002 Traceability serial number log
F-852-003 Traceability label
F-854-001 Storage inspection report
F-854-002 Packing slip / Invoice
F-857-001 Service projects log
F-857-002 Project inspection completion report
F-870-001 Nonconformance report – NCR
F-910-001 Production-Monitoring, measuring, and analysis table
F-910-002 QMS-Monitoring, measuring, and analysis table
F-910-004 Inspection report
F-911-001 Frequency distribution report
F-912-001 Customer survey and analysis
F-913-001 Root cause analysis action plan
F-920-001 Applicable procedure by work area
F-920-002 Internal audit checklist
F-920-003 Audit plan
F-920-004 Audit report
F-930-001 Management review agenda
F-930-002 Management review output report
F-1010-001 Data analysis worksheet
F-1020-001 Corrective action request – CAR

 

Product Details

Product Type: Digital

Price:$397.00

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Which version is right for me?

Choose IATF 16949:2016 to create a new IATF 16949 Quality Management System

Choose TS 16949:2009 to IATF 16949:2016 QMS to modify your existing TS 16949:2009 QMS to meet the IATF 16949:2016 requirements

Choose ISO 9001:2015 to IATF 16949:2016 QMS Upgrade to modify your existing ISO 9001:2015 to meet the IATF 16949:2016 requirements

If you plan to reconfigure your existing quality manual completely by yourself, you can use either of the Upgrade Instructions to create everything on your own. They will tell you where to make the changes but will NOT provide any procedure or form templates for the new requirements.

Price Each IATF 16949
QMS
TS 16949 to IATF 16949
QMS
ISO 9001 to IATF 16949
QMS
Your Price
IATF 16949:2016 Quality Manual $97.00 N N N
IATF 16949:2016 Procedures $300.00 N N N
IATF 16949:2016 Forms $100.00 N N N
IATF 16949:2016 Flow Charts $75.00 N N N
TS 16949:2009 to IATF 16949:2016 QMS Upgrade Instructions $199.00 N
ISO 9001:2015 to IATF 16949:2016 QMS Upgrade Instructions $199.00 N
Support FREE N N N
Your Price

Specific Contents

Procedures
P-1010 Improvement
P-1020 Nonconformity and corrective action
P-400 Organizational context
P-500 Leadership
P-600 Planning for the Quality Management System
P-612 Preventive action
P-710 Resource management
P-715 Control of monitoring and measuring equipment
P-720 Competence and awareness
P-740 Communication
P-750 Control of documented information
P-810 Operational planning and control
P-820 Customer related processes
P-830 Design and development of products
P-831 Design and development of manufacturing processes
P-840 Control of external providers
P-851 Control of production
P-852 Identification and traceability
P-854 Preservation
P-857 Other operational control
P-860 Release of products and services
P-870 Control of nonconforming outputs
P-910 Monitoring, measurement, analysis and evaluation
P-911 Statistical techniques
P-912 Customer satisfaction
P-913 Root cause analysis
P-920 Internal audit
P-930 Management review
Forms
F-1010-001 Data analysis worksheet
F-1020-001 Corrective action request - CAR
F-440-001 QMS-Process identification worksheet
F-440-002 Organizational context worksheet
F-440-003 Product safety worksheet
F-610-001 Risk and opportunity worksheet
F-612-001 Contingency plans worksheet
F-620-001 Quality objectives planning record
F-710-001 Equipment problem report
F-710-002 Resource maintenance record
F-715-001 Equipment calibration list
F-715-001 Laboratory requirements worksheet
F-720-001 Training action plan
F-720-002 Group training record
F-720-003 Job description
F-720-004 Employee training summary
F-720-005 Auditor competency worksheet
F-740-001 Comment and suggestion report
F-750-001 List of documented information
F-750-002 Records matrix
F-750-003 Master documentation lists
F-750-004 Quality records table
F-750-005 Document change request form
F-750-006 Document revision checklist
F-750-007 Software inventory spreadsheet
F-810-002 Project planning worksheet
F-820-001 Client assessment report
F-820-002 Production order
F-830-001 Design plan
F-830-002 Design review record
F-830-003 Design change form
F-840-001 Provider assessment report
F-840-002 List of acceptable sources
F-840-003 Provider corrective action request - PCAR
F-840-004 Purchase requisition
F-840-005 Purchase order
F-840-006 Business agreement - contract
F-851-001 Process routing sheet - summary
F-851-002 Process routing sheet - summary
F-851-003 Process validation worksheet
F-851-006 External property control log
F-851-010 Control plan worksheet
F-852-001 Identification tag
F-852-002 Traceability serial number log
F-852-003 Traceability label
F-854-001 Storage inspection report
F-854-002 Packing slip / Invoice
F-857-001 Service projects log
F-857-002 Project inspection completion report
F-870-001 Nonconformance report - NCR
F-910-001 Production-Monitoring, measuring, and analysis table
F-910-002 QMS-Monitoring, measuring, and analysis table
F-910-004 Inspection report
F-911-001 Frequency distribution report
F-912-001 Customer survey and analysis
F-913-001 Root cause analysis action plan
F-920-001 Applicable procedure by work area
F-920-002 Internal audit checklist
F-920-003 Audit plan
F-920-004 Audit report
F-930-001 Management review agenda
F-930-002 Management review output report
Attachments & Work Instructions
A-510-001 Corporate responsibility policies
A-520-001 Quality policy
A-530-001 Organization chart
A-600-001 PDCA guidelines
A-715-001 Calibration activities and records guidelines
WI-750-001 Document numbering system
Flow Charts
FD-440-001 Process interaction flow diagram
FD-510-001 Business process map
FD-810-002 Process flow diagram
FD-850-001 Operations-Production and Service