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"The Quality Manual is one of the most useful documents because unless you have actually put one of these together before how would you know where to start! Once I started looking through all that is included in the package, I realized that The 9000 Store has thought of everything."
- Debbie Elderton, ICE Communications
Save the time and resources required to design and document an ISO 9001 Quality Management System. The 9000 Store has created most of it for you. The key to an effective Quality Management System is designing the documentation for efficiency and ease of use. Our documents, edited by professional technical writers, have been written in Microsoft Word so you can easily edit and customize them to make them your own. When you have questions, our experts are only an email away.
BONUS: Includes 1 free Online ISO 9001:2008 Basic Training session! ($24 value)
Begin with this fully documented 36 page ISO 9001:2008 Quality Manual that has been used for successful registrations across the globe. You will appreciate its ease of use - simple yet thorough. Why make it complicated?
Although our products are easy to use, we still offer World Class Support for your project - for FREE!
Our products have been proven over 10 years - longer than anyone else - and have helped companies around the world become certified. We don't flood our packages with unnecessary forms and other "fluff" to make them look complete. Ours ARE complete, and get the job done.
Experienced ISO professionals are available to answer questions and help you develop and implement your QMS.
According to the ISO 9001 Standard: the Quality Manual needs to refer to the processes which make up The Quality Management System (QMS). Our Quality Manual already references our procedures and forms, saving you much time and money. You will need to add procedures and forms to your QMS. Why create your own? Upgrade to the Quality Manual and Procedures packet and use ours.
How Much Documentation Do You Need For Your ISO 9000 process?
Much depends on the size and complexity of your organization. You should have enough procedures to cover each section of the standard that applies to your business.
The ISO/IAF Guidelines says: "The auditee/auditor considers that each clause or sub-clause of ISO 9001 must be defined as a separate process". Do you purchase anything that could have an impact on meeting the customers' requirements? Then you'll need a Purchasing Procedure to describe section 7.4 - yet that isn't "required".
There are actually 20 different related (ISO 9000) processes called out in the standard. The 9000 Store has designed clearly written procedures to describe each section of the standard. That is why our QMS process is better than the rest - we cover the entire standard. Don't think you can only provide a few procedures and call it an ISO 9000 QMS. The result can be a very poor ISO 9000 process. Is it worth the savings?
ISO 9001 has 20 requirements. All of our QMS products address the requirements in the Quality Manual, but the different versions provide separate procedures for more detailed processes.
Which QMS is right for me?
ISO 9001 also suggests statistical tools for your Corrective/Preventive Action and sampling. We have included optional procedures for this in the Complete QMS.
|Which version is right for me?|
|Quality Manual||Lean QMS||Service QMS||Complete QMS|
|Free Support throughout your project!|
|4 PowerPoint Presentations|
|Complete Quality Manual|
|2 hour Online ISO 9001 Project Manager Training|
|Level 2 Procedures||6||13||22|
|Forms, Tables, & Attachments for Records||40||40||41|
|Templates for Processes & Work Instructions||3||3||3|
|ISO 9001 Process Flow Charts||3||13||27|
|Quality Policy Sample & Template|
|Flowchart Software Included *
6 months free subscription to LucidChart Pro Flowchart software. LucidChart allows you to import and export MS Visio files and edit as needed.
|Mandatory Procedures||Quality Manual||Lean QMS||Service QMS||Complete QMS|
|Sec. 4.2.3 Document Control|
|Sec 4.2.4 Control of Quality Records|
|Sec. 8.2.2 Internal Audits|
|Sec. 8.3.0 Control of Nonconforming Product|
|Sec. 8.5.2 Corrective Action|
|Sec 8.5.3 Preventive Action|
|Additional Procedures for the following sections:||Quality Manual||Lean QMS||Service QMS||Complete QMS|
|Sec 5.0.0 Management Responsibility|
|Sec. 6.2.2 Competence, Awareness and Training|
|Sec. 6.3.0 Infrastructure|
|Sec. 7.1.0 Planning of Product Realization Processes|
|Sec. 7.3.0 Design and Development|
|Sec. 7.4.0 Purchasing|
|Sec. 7.2.0 Customer Related Processes|
|Sec. 7.5.0 Control of Production and Service|
|Sec. 7.5.3 Identification and Traceability|
|Sec. 7.5.4 Customer Property|
|Sec. 7.5.5 Preservation of Product|
|Sec. 7.6.0 Control of Monitoring and Measuring Equipment|
|Sec. 8.2.1 Monitoring, Measuring and Analysis of Customer Satisfaction|
|Sec. 8.2.4 Monitoring, Measuring & Analysis of Product & Realization Processes|
|Sec. 8.4.1 Root Cause Analysis|
|Sec. 8.4.0 Statistical Techniques|
|Forms||Quality Manual||Lean QMS||Service QMS||Complete QMS|
|F-423-001 Master Document List|
|F-423-002 Software Inventory Spreadsheet|
|F-423-003 Document Change Request Form|
|F-423-004 Document Revision Checklist|
|F-424-001 Quality Records Table|
|F-500-002 Key Process Master List|
|F-500-001 QMS Monitoring, Measuring and Analysis Table|
|A-500-001 Quality Policy|
|A-550-001 Organization Chart|
|F-560-001 Management Review Agenda|
|F-560-002 Management Review Checklist|
|F-622-001 Training Action Plan|
|F-622-002 Group Training Record|
|F-622-003 Job Description Form|
|F-630-001 Equipment Problem Report|
|F-630-002 Equipment Maintenance Record|
|F-700-005 Clause 7 Inclusion-Exclusion Worksheet|
|F-710-001 Quality Planning Table|
|A-710-010 Process Flow Chart|
|F-720-001 Client Assessment Memo|
|F-730-001 Design Plan|
|F-730-002 Design Review Record|
|F-730-003 Design Change|
|F-740-001 Supplier Quality Reports|
|F-740-002 Supplier Corrective Action Request|
|F-740-003 Approved Supplier List|
|F-750-001 Process Routing - Summary|
|F-750-002 Process Routing - Detail|
|F-752-001 Process Validation Worksheet|
|F-753-001 Traceability Serial Number Log|
|F-754-005 Customer Property Control Log|
|F-755-001 Storage Inspection Report|
|F-760-001 Equipment List|
|F-821-001 Customer Satisfaction Survey|
|F-822-001 Internal Audit Plan|
|F-822-002 Internal Audit Report|
|F-822-003 Applicable Procedures by Work Area|
|F-822-004 Audit Point Checklist|
|F-824-001 Product Realization Monitoring, Measuring and Analysis Table|
|F-830-001 Rejected Material/Disposition Report-NCR|
|F-841-001 Root Cause Analysis and Action Plan|
|F-852-001 Corrective/Preventive Action Request|
|Flow Diagrams||Quality Manual||Lean QMS||Service QMS||Complete QMS|
|FD-400 Structure of the QMS|
|FD-410 Business Process Map|
|FD 415 Management Functions|
|FD-423 Control of Documents|
|FD-424 Control of Records|
|FD-500 Management Responsibility|
|FD-510 Management Commitment|
|FD-540 Planning Product Realization, Monitoring and Measurement|
|FD-545 Quality Objectives|
|FD-600 Resource Management|
|FD-610 Resource Management|
|FD-700 Realization of Product|
|FD-710 Manufacturing Process|
|FD-714 Product Realization Quality Plan|
|FD-720 Customer Related Processes|
|FD-730 Design and Development|
|FD-731 Project Timing - Design and Development|
|FD-732 Sequence of Development|
|FD-750 Process Control|
|FD-751 Process Control Steps|
|FD-752 Post Delivery Service Process|
|FD-753 Identification and Traceability|
|FD-800 Measurement, Analysis and Improvement|
|FD 840 Continual Improvement|
|FD-852 Corrective Action|