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We are attempting to revamp our document control system in anticipation of ISO 9001 certification. We are struggling with whether or not to separate the approval processes of label artwork (we sell retail pool products), engineering drawings for parts and assemblies, and QMS documents such as SOPs, production records, training records, etc.
I'd like to know what other people have experienced. Was it easier to have 3 different approval processes? Could one process be designed to control all 3?
Thanks,
Ian
I'd like to know what other people have experienced. Was it easier to have 3 different approval processes? Could one process be designed to control all 3?
Thanks,
Ian