S
shawnann
I'm going to post this here because we are in the process of getting ISO 17025 certified, but I guess the question could go for any certifications that require a quality manual.
We all know that a quality manual is required, as it states in the instructions for the application for accreditation that you need to "Create and implement a Quality Manual and Management System policies and procedures that meet the ISO/IEC 17025:2005 and A2LA requirements."
So my question is, how elaborate does the quality manual have to be? When we got our ISO 9001 certification, we for the most part typed word for word the international standard, with the exception of creating a couple pages at the beginning and this was acceptable. We were also told we could combine the quality manual to our procedures manual and eliminate the part of the quality manual that was word for word of the international standard. Can we just create those "extra pages" and use the international standard (as is) as our quality manual? This would save a lot of time typing something that is already in print and paper that really isn't needed to be printed on.
In other words, create a quality policy (or quality pages), that lists the scope of the laboratory/company, the organizational overview-mission (who we are, etc) and then refer to the international standard for the actual quality manual.
We all know that a quality manual is required, as it states in the instructions for the application for accreditation that you need to "Create and implement a Quality Manual and Management System policies and procedures that meet the ISO/IEC 17025:2005 and A2LA requirements."
So my question is, how elaborate does the quality manual have to be? When we got our ISO 9001 certification, we for the most part typed word for word the international standard, with the exception of creating a couple pages at the beginning and this was acceptable. We were also told we could combine the quality manual to our procedures manual and eliminate the part of the quality manual that was word for word of the international standard. Can we just create those "extra pages" and use the international standard (as is) as our quality manual? This would save a lot of time typing something that is already in print and paper that really isn't needed to be printed on.
In other words, create a quality policy (or quality pages), that lists the scope of the laboratory/company, the organizational overview-mission (who we are, etc) and then refer to the international standard for the actual quality manual.
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