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How can I evidence the failure test of the error-proof devices?
During our Stage 1 document review, our auditor said that we should consider drastically reducing the Quality Manual, which I agree with. What is the minimum size and scope that a QMS Manual should look like? For example, why should anyone document in the manual the actual standard? I have one I have put weeks into, that is blended between ISO:9001 / AS9100 / IATF16949 however it does reek of a regurgitation of the standards. What is the best simple approach?