The ISO 9001 documentation is at the core of any ISO 9001 Quality Management System (QMS). What makes the documentation so important? There are two important aspects:
(2) your company has to actually do everything that is contained in your company's ISO 9001 documentation.
Your company needs a comprehensive set of ISO 9001 documents and to actually conduct its business in accordance with them. Consequently, it is crucial that the documentation not only meets ISO 9001:2015 requirements, but is efficient and doesn't increase company bureaucracy. This is a very important consideration as we have seen far too many companies invest excessive employee hours and money in maintaining an overly complicated and bureaucratic QMS. We therefore urge you to keep your documentation as simple and efficient as possible. If you use templates or consultants for your ISO 9001 documentation, be sure to choose wisely.
The procedures form the essence of the ISO 9001 documentation: they explicitly describe how numerous processes within the company must be performed, and who is responsible for them. Ideally, the procedures are combined in a single user-friendly document (a "procedures manual" or "quality management manual", or similar). ISO 9001:2015 sets the requirements for the procedures and their content in many clauses; the requirements are not always explicit. We recommend you have procedures covering most or all applicable ISO 9001:2015 requirements.
The quality policy defines company's stance re: quality and customer satisfaction. As such, the ISO 9001 quality policy is the overall guiding principle. The content of the quality policy must meet the requirements of ISO 9001:2015 section 5.2.
The process flowchart describes how the various processes of the ISO 9001 QMS interact with each other. The process flowchart is required in ISO 9001:2015 section 4.4.
The scope statement defines the application and boundaries of the Quality Management System within the company. The scope statement is required in ISO 9001:2015 section 4.3.
Work instructions are the most detailed and company-specific of all ISO 9001 documents: they describe in detail how particular tasks must be performed and are typically written by the people who perform the actual work. ISO 9001:2015 requires work instructions only where they add real value to the company; it is a common misconception that every task in the company needs to be documented. Work instructions are required by ISO 9001:2015 section 8.5.1.
Records are different from the above documents, all of which provide directions on how to conduct business. Records, on the other hand, are evidence of things done. ISO 9001:2015 contains numerous explicit requirements on records, plus requirements for many more undefined records.
Forms are optional
ISO 9001:2015 does NOT contain requirements on using forms. In fact, it would not be a violation of ISO 9001:2015 requirements not to have any forms at all. However, good forms provide many benefits to any business, ranging from time savings to consistency. Using forms can be a tremendous help creating the various records that ISO 9001:2015 requires. The best forms even act as instructions when they guide the user through the process of providing the requested information.
How about the Quality Manual?
Previous revisions of ISO 9001 required a Quality Manual which contained the overall description of the company's QMS. ISO 9001:2015 no longer requires such a manual. However, some companies choose to develop a Quality Manual for marketing purposes and to provide external parties with general information about their Quality Management System without revealing their proprietary processes.
ISO 9001:2015 does not require any particular format or layout;
referencing every document and form to each other is not required;
there are no requirements regarding introductory paragraphs to procedures;
and there are certainly no requirements saying that the documentation needs to be complicated and hard to understand.
Remember that the ISO 9001 documentation is supposed to provide instructions on how to operate your company's ISO 9001 Quality Management System. The best documentation is easy to understand and user-friendly; the easier it is to follow, the better.
We have seen many companies making the mistake of creating numerous different documents and referencing in each of them all other pertinent documents. This approach not only causes redundancies, but is far from user-friendly and usually the beginning of an overly bureaucratic QMS.
We recommend creating user-friendly ISO 9001 documentation by combining the different documentation requirements (i.e, procedures, quality policy, scope and process flowchart) as much as possible into a single comprehensive manual (ie, an "ISO 9001 QMS manual", "procedures manual" or "quality management manual", etc). This reduces repetition and bureaucracy, and saves time implementing the QMS.
Good ISO 9001 documentation always keeps the user of the document in mind: remember too that while some users like instructions in the form of pictures, others prefer flowcharts. Few enjoy reading passages of long, convoluted text.
A word of caution
If you chose templates for your ISO 9001 documentation, always look at samples and follow our practical evaluation tips. If they seem overly complicated and/or hard to understand, they will be of little use to your company and employees. If an ISO 9000 consultant insists on writing documentation that you don't understand, chances are that this documentation will be useless at best or a burden to your company's performance at worst.