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Is it necessary to have both an operating procedure and a quality procedure? I just started at a new company that is ISO 9001-2000 certified. I am noticing that for certain things such as Document Control and Control of NonconformingProduct that their system has both a QP and SOP. There does not appear to be any real fundamental difference between the procedures. I come from a TS16949 system and this just doesn't make any sense to me. Please help me understand why this is necessary!