But if you one of your QMS documents makes reference to 17025 then you should have a process to assure the current revision is on hand when the Quality Manager is asked by a 2nd party or 3rd party auditor to produce a controlled copy of this document.
Yes, if the organization works to 17025, or if the quality manager would like to have a comprehensive understanding of the management systems required for operating a test/calibration lab.
For the majority of quality managers the answer will likely be no.
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