Once upon a time, in previous employment we had as part of our Document Control/Change Procedure an explanation of how someone would notify Document Control that a procedure was no longer needed along with an explanation as to why it wasn't needed. Then if approved, Document control would notify all users of that procedure that it was no longer in use. Fast forward several years, I am with a new company. We are going for ISO9001 but do not have a medical device component to it like my previous job. I still think we need to have a procedure/process written within our Doc Control procedure explaining this part.
Am I thinking too much with my FDA brain? Or is this perfectly justifiable in the ISO world also?
Thank you! Melissa
Am I thinking too much with my FDA brain? Or is this perfectly justifiable in the ISO world also?
Thank you! Melissa