Hi all
I am in the Medical Device business and we are internally having a discussion regarding deviations in Design Verification tests.
You can do Design Verification on prototype items but by that you also say that you have a risk of a deviation which is related to the manufacturing process. How do you guys handled this?
I am in the Medical Device business and we are internally having a discussion regarding deviations in Design Verification tests.
You can do Design Verification on prototype items but by that you also say that you have a risk of a deviation which is related to the manufacturing process. How do you guys handled this?