Welcome to ISO 9000 Resources, the source for cost-effective battle-tested quality system information. Our experienced staff of consultants has taken the guess work out of ISO 9001 development by developing a full range of ISO 9001 products. Some of this information is derived our our work with the ReGenPod whole-body photobiomodulation system and the FDA/ISO requirements. All our products are based on years of practical real-world experience working. Based on this experience, our product are more than just compliant, they are effective AND efficient. Our products will save your company money and time while helping focus your resources to accomplish your goal on time and on budget. All our products are 100% guaranteed.


ISO 9001 Starter Kit ISO 9001 Documentation Kit ISO 9001 Total Quality System
Our Starter Kit is the perfect solution for companies just starting the implementation process. This kit will help jump-start a successful ISO project. Our Documentation Kit includes a proven quality manual and all the most critical procedures, forms and documents. This package contains the backbone of a world-class quality system Our Total Quality Management System includes every manual, flow chart, plan, form, schedule, procedure and guide in our library. Our ultimate resource for creating an effective and efficient quality system.
$45
$195
$495 Now $295

All our products are 100% satisfaction guaranteed.

New To ISO? Try Our 17-step ISO Implementation Project Plan

1. Get the Big Picture
The first step is to understand the basic elements of ISO 9001:2010 including costs and how it changes the way the company does business. Our ISO 9001 starter kit is one of the best tools for getting started. If your company is lacking a significant portion of an ISO compliant quality system, you want to purchase a turnkey Quality Management System (QMS) to accelerate the project. At any point in the process, you can get ISO 9001 consulting to help with the system design. Perform a QMS evaluation to estimate resources for the project. Create and approve a justification for the ISO project (just like a design project).

2. Evaluate Your Quality System and Start The Implementation Project
Assess your current quality system using a gap analysis check sheet and then make sure that management will commit a sufficient level of resources to complete the project. Review the implementation cost articles to get the big picture of the cost. Save the gap analysis for later use as an internal audit (once you have an internal audit system)

3. Develop The Implementation Plan And Quality Goals
Develop the quality objectives, quality statement and project scope. Use the samples on this web site as a basis for developing quantifiable quality objectives and a quality statement that is memorable and fulfills the ISO requirements for a customer focus. Create an implementation plan with a timeline, cost and resources. Submit the plan to management and get approval.

4. Create The Documentation Control Procedures
Establish your document control first so that you have an established system for creating your other documents and for maintaining revision control of all quality documents. All the documents that you create should have unique tracking numbers and revisions. The documentation control process is used in conjunction with the engineering change order (ECO) system to maintain revision control.

5. Create The Corrective and Preventive Actions System
In most companies the corrective and preventive actions system is known as the Engineering Request and Order (ECR/ECO) system. Use this system to approve and release all documentation in conjunction with the documentation control procedure. The ECR/ECO system is an excellent area for automation.

6. Generate A Quality Manual
Purchase an ISO 9001 quality manual or copy the sample quality manual from this site. Adapt the manual to include your own quality statement and any special needs. Generate the product flow chart and organization chart for the company as part of the quality manual. The organizational chart should show the quality responsibilities for key personnel like the Quality System Management Representative (QSMR).

7. Start Training Employees and Maintaining Training Records
Write the ISO 9001 training procedure and start maintaining a training records notebook. Perform ISO awareness training and log the training in everyone’s training records. Once you have created all your procedures and work instruction, you will record the training of these processes in this notebook.

8. Inventory and Customer Fulfillment Documentation
Create your inventory control, service and customer-fulfillment procedures. You will need to build some history of processing inventory for any internal audit to be worthwhile.

9. Purchasing Control Documentation
Create your purchasing control procedures. Complete some transactions including ordering, receiving, building and shipping product to demonstrate the complete purchasing and inventory management system. Some of the inventory should be nonconforming so the auditor can follow both good and bad materials through the process.

10. Maintaining Nonconforming Materials
Create your nonconforming materials procedure and begin tracking defects in a central database, file or notebook. Make sure that everyone properly labels nonconforming materials. Build some history of nonconforming materials (including corrective actions) before the next internal audit.

11. Design Control
Create your design control procedure and then generate notebooks for all current design projects. Start using revision control on the project specifications. Hopefully you will have some short-term projects that can be completed prior to the next internal audit. The company should have a completed design notebook for the certification audit.

12. Calibration And Maintenance Of Equipment
Implement your calibration and maintenance procedures. Enter all production equipment into a database or spreadsheet. Set up a calibration schedule and have all appropriate equipment calibrated. Record the status of each device in the database.

13. Detailed Work Instructions
The Company now has most of your key operational systems in place. Now you can create your detailed work instructions that are used for process control. These procedures may be very simple and may be created dynamically or the processes may be performed by "qualified" personnel without work instructions.

14. Management Review
Perform a management review meeting. Present the quality data that has been collected and discuss goals and ISO status. Log this meeting in your management review notebook.

15. Internal Audit And Closure
You can purchase a turnkey internal audit package or use the internal audit samples on this site. Create the internal audit program including an annual schedule. Choose an internal audit team and perform an internal audit. This audit should be logged in the audit records and should generate corrective actions in the engineering change order system. Close all these corrective actions. If possible, perform another management review to present the status of the new quality system.

16. The Certification Audit
At this point, the Company will have records to show that there is a Quality Systems in place and working so you can choose a Registrar and schedule the certification audit.

17. Continuous Improvement
At successful companies, the improvements never end. ISO 9001 and non-ISO companies need to focus on continuous improvement of the quality of their products, processes and quality system.

Testimonials:

"This looks like it's exactly what we needed. Short and sweet and not cumbersome." - Henry at MAETS 2011