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ISO 9001:2015 Premium Documentation Toolkit – 45+ Documents!

Original price was: 650,00 $.Current price is: 79,00 $.

This is the most comprehensive ISO 9001document toolkit currently available.

The documents are created in Microsoft Office format and are ready to be tailored to your organization’s specific needs. As well as standard format and contents, the ISO 27001 template documents include example text that is clearly highlighted to illustrate the type of information that needs to be given regarding your organization. Full example documents are also included to help you with your implementation.

Description

ISO9001:2015 Premium Toolkit

This is the most comprehensive ISO 9001:2015 document toolkit currently available.

The documents are created in Microsoft Office format and are ready to be tailored to your organization’s specific needs. As well as standard format and contents, the ISO 9001 template documents include example text that is clearly highlighted to illustrate the type of information that needs to be given regarding your organization. Full example documents are also included to help you with your implementation.

Written by a qualified auditor with over 18 years of experience in Quality Management, our toolkit provides years of experience and knowledge in an easy-to-implement format.

With quality and quantity included, this award-winning toolkit covers everything an organization will need, so you can use it first to become certified to the standard, and then to develop and continually improve your Quality Management System (QMS).

 

What is included within the ISO 9001:2015 toolkit?

  • 45+ template documents – including policies, procedures, controls, checklists, tools, presentations and other useful documentation
  • Available as an instant download after purchase

45+ Templates

Quality Management System (QMS) Documentation pack

A full and comprehensive documentation pack to help clients, consultants and service providers achieve ISO 9001:2015 successfully.

Pack folder structure:

  • P-QMS-01 Procedure for Determining the Context and Interested parties
  • P-QMS-02 QMS Objectives
  • P-QMS-03 QMS Communication, Participation and Consultation Procedure
  • P-QMS-04 Procedure for Risk and Opportunity
  • P-QMS-05 Procedure for Legal Requirement
  • P-QMS-06 Procedure for Competence, Training and Awareness
  • P-QMS-07 Procedure for Control of Documented Information
  • P-QMS-08 Procedure for Control of Operation
  • P-QMS-09 Procedure for Calibration
  • P-QMS-11 Procedure for Performance Monitoring and Evaluation of Compliance
  • P-QMS-12 Procedure for Internal Audit
  • P-QMS-13 Procedure for Management Review
  • P-QMS-14 Procedure for Non Conformity Reporting and Corrective action
  • P-QMS-15 Procedure for Continual Improvement
  • P-QMS-16 Procedure for Management of Change
  • P-QMS-17 Procedure for Special Processes
  • P-QMS-18 Procedure for Product Identification _ Traceability
  • P-QMS-19 Procedure for Outsourced Processes
  • P-QMS-20 Procedure for Design and development
  • P-QMS-21 Procedure for Preservation
  • P-QMS-22 Procedure for Purchasing
  • P-QMS-23 Procedure for Control of Third Party Property
  • P-QMS-24 Quality Management System Policy
  • P-QMS-25 Quality Management System Manual
  • P-QMS-26 Internal Audit Checklist
  • P-QMS-27 Quality Management System Assessment Checklist

List of all documents:

  1. QMS Context Log and list of Interested Parties.docx
  2. Objectives and targets master sheet.xlsx
  3. Objective and target change request form.xls
  4. Training Matrix.xlsx
  5. Training needs analysis form.doc
  6. MRM Minutes of Meeting.docx
  7. Document Change Request Form.docx
  8. Internal Audit Schedule.xlsx
  9. Internal Audit Report.xlsx
  10. Corrective Action Report (CAR).docx
  11. Lesson Learned Form.xls
  12. Change Request Form.docx
  13. Design Control Form.docx
  14. Requisition Form.docx
  15. Internal Audit Checklist ISO9001-2015.docx
  16. ISO 9001-2015 QMS Assessment Checklist.pdf
  17. ISO9001-2015 Quality management systems – Requirements Standard Document.PDF
  18. Procedure for Management of Change.docx
  19. Procedure for Determining the Context and Interested parties.docx
  20. QMS Objectives V1.0.docx
  21. QMS Communication Procedure.docx
  22. Procedure for Risk and Opportunity.docx
  23. Procedure for Legal Requirement.docx
  24. Procedure for Competence, Training and Awareness.docx
  25. Procedure for Control of Documented Information.docx
  26. Procedure for Control of Operations.docx
  27. Procedure for Calibration.docx
  28. Procedure for Performance Monitoring and Evaluation of Compliance.docx
  29. Procedure for Internal Audit.docx
  30. Procedure for Management Review.docx
  31. Procedure for Continual Improvement.docx
  32. Procedure for Special Processess.docx
  33. Procedure for Product Identification _ Traceability.docx
  34. Procedure for Outsourced Processes.docx
  35. Procedure for Design and development.docx
  36. Procedure for Preservation.docx
  37. Procedure for Purchasing.docx
  38. Procedure for Control of Third Party Property.docx
  39. QMS Manual V1.0.docx
  40. QMS Policy V1.0.docx
  41. Risk and Opportunity Register.xlsx
  42. Legal Register.xlsx
  43. Training Register.xlsx
  44. External Document Register.docx
  45. Document Master Register.xlsx
  46. Calibration Register.docx
  47. Calibration Monitoring and Production Software Validation Register.docx
  48. Change Management Register.xlsx
  49. SWOT Analysis Template.docx

 

All GovernanaceDocs documents are developed based on well-known standards such as NIST CSF, ISO 27001, ISO9001, ISO 22301, PCI-DSS and HIPAA.

Hence, You just need to download and selected document and add your company name and logo.

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