Re: MRR coordinator
Sorry, I cannot give great detail on the acronym. It is a post with a medical devices company. They are governed by ISO 9001:2000 and 13485(2003).
I was told that the main part of it focussed on non-conformities.
I found an ISO checklist for 9001/13485.
would the material rejection report be generated to cover clause 8.3? of 13485?
i.e. "Records of the nature of nonconformities and any subsequent actions taken, including concessions obtained, shall be maintained "
I have to apologise, I have never worked with ISO's before so I can only go on what I've read