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DOCUMENTATION OPTIONS

ISO Quality Manuals offers several template options to meet your organizations quality documentation needs. Our quality documentation has been the successful choice for many businesses, both large and small, and continues to prove it is the best choice for quick implementation and fast ISO certification. Successfully applied to service, manufacturing and distribution companies.

Why This Documentation Will Work for You

Your Specific Industry Documentation

Templates	Policies	Procedures Forms	Email/Phone Support	Instructions	Pre-Assessment worksheet	Price
Quality Control Manual						$149
Quality Procedures Manual						$169
Complete Doc Package						$299

Documentation will determine the success of your program. It must

Satisfy all requirements of ISO

Be easily revised

Follow a recognized format

Have the ability to grow

Be simple to read and understand

Why This Documentation Will Work for You

Many clients seek assistance in creating documentation specific for their business and industry. While this request makes sense, it is important to understand what makes up a documented quality program. Quality documentation is divided into 2 parts or elements. Understanding this is very important to establish your program affordably. While it is reasonable to expect industry specific documentation to be required, the core elements of any Quality Management System are consistent and the same. Regardless of the type or size of your company your quality program will include the same elements used by everyone. This is the reason we can say with confidence this program documentation will work for your organization.

What About Documentation Specific for my Company?

The general activities involved in delivery of products and/or services are covered by the ISO guidelines in Section 7. Titled Product Realization the writers were careful to word this section in a manner that will work for any type of business. The result is an ISO standard applicable for all quality management systems regardless of business type.

Our Quality Control Manual details the policies required to fulfill the intent of ISO product realization. The policy specifies what must be done to ensure controls are in place for these activities, however the details regarding how you accomplish your product realization may be included in supporting documents like procedures and flow charts. As a result the manual presents a complete policy document, that may be issued immediately after receipt and template modifications are complete.

The specific processes involved in your business may be detailed in supporting documents and included in the Quality Procedures Manual .

Start With A Solid Foundation

You must begin with a solid foundation. A documentation package that covers the required Core Elements in the simplest method possible. A package that you can easily modify to improve along the way and especially important, a package you can add your industry specific elements to as they are developed. Our Documentation Package provides this solid foundation.

Save money and time by purchasing documentation that contains the core elements of your quality management system. You will have a documented format and a solid foundation for your system.

With the use of our Quality Documentation, you may dedicate your time to identifying the industry specific documentation that should be included with your program and adding it to the foundation provided.

A Quality Documentation program typically include 2 levels of documentation, as detailed below.

The Quality Control Manual contains your company policies and will be complete and ready to issue after the simple instructions are followed to add your logo and specific company information to the text..
The Quality Procedures Manual will include the 6 required procedures, forms and records you will need to accomplish ISO compliance. This is an internal document and is not usually issued to clients. This is the manual you will add your industry specific documentation to.

The Quality Control Manual follows the ISO format and includes all sections of the 9001:2008 requirements. Supporting procedures and records offered represent the minimum requirements of ISO. There are no documents considered optional, therefore the user is not required to sort through a list of documentation or make a determination on minimum requirements for the basic quality management system. The clients existing procedures and/or records may be easily added to the basic package.

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