Cookey5599
Registered
Good Morning
Am putting together an operational risk management process in accordance with Rev D 8.1.1 and wondered if simply following the APQP process linked to a central register was enough to satisfy this requirement? We are a sub con CNC manufacturing facility with no design scope.
As an alternative We have lots of processes that consider operational risk such as Contract review, Process/Product FMEA, Quality clinic outputs, but not a centralized log as I just think it is duplicating information.
The IAQG have lots of information and an example risk register that unfortunately is not a working version so I have asked them if they could provide this as part of the presentation
Thanks in advance for any feedback/Assistance
Am putting together an operational risk management process in accordance with Rev D 8.1.1 and wondered if simply following the APQP process linked to a central register was enough to satisfy this requirement? We are a sub con CNC manufacturing facility with no design scope.
As an alternative We have lots of processes that consider operational risk such as Contract review, Process/Product FMEA, Quality clinic outputs, but not a centralized log as I just think it is duplicating information.
The IAQG have lots of information and an example risk register that unfortunately is not a working version so I have asked them if they could provide this as part of the presentation
Thanks in advance for any feedback/Assistance