Dumpsterdude
Registered
Hello,
I am currently in the process of updating a QMS, rewriting procedures etc, I have come across a hurdle that I need some assistance with. The company I am currently with is an ISO 9001: 2015 / AS9100D company, we are currently engaged in contracts for the defence industry, my hurdle is as follows, I am confident with the updating of the QMS based on the guide lines of ISO and AS, but we have a lot of documentation that is deemed to be of a confidential / sensitive nature and I am unsure how to control this - I am aware we need to add controls in place - any ideas
I am currently in the process of updating a QMS, rewriting procedures etc, I have come across a hurdle that I need some assistance with. The company I am currently with is an ISO 9001: 2015 / AS9100D company, we are currently engaged in contracts for the defence industry, my hurdle is as follows, I am confident with the updating of the QMS based on the guide lines of ISO and AS, but we have a lot of documentation that is deemed to be of a confidential / sensitive nature and I am unsure how to control this - I am aware we need to add controls in place - any ideas