S
Steven Sulkin
In a recent customer audit, I learned about a different approach to control plans. I would appreciate learning how others are tackling this requirement. So, far this is what I have seen:
One control plan for every one or two tier QS9000 firm only.
One to a few control plans that are generic enough to represent the facility. All exceptions (for individual products) are noted in appendices.
Anyone doing it differently? What process have you found to be value added (i.e. help with improvement rather than just meet the requirements)?
If you have a procedure please outline in post or email.
Thanks in advance.
One control plan for every one or two tier QS9000 firm only.
One to a few control plans that are generic enough to represent the facility. All exceptions (for individual products) are noted in appendices.
Anyone doing it differently? What process have you found to be value added (i.e. help with improvement rather than just meet the requirements)?
If you have a procedure please outline in post or email.
Thanks in advance.