L
Does anyone know of anywhere in the FDA's CFR or other "Guidance" documents a reference to checking for "patent infringement" during the Design Control process? Shouldn't all medical device manufacturing companies point to an SOP or somewhere in the CFR for a check of "patent infringement" during some phase of the Design Process?
As always, I am grateful for any and all response!
Best Regards!
LEE
As always, I am grateful for any and all response!
Best Regards!
LEE