I am Himang having 6 years of experience in the medical device industry with 3+ years of experience in medical device development and manufacturing environment.
I have worked as Quality engineer in one company while as R&D Engineer in another but was not able to connect the dots between the two experience. I mean, how Design transfer occurs? What needs to be considered while transferring the prototype designed in the R&D into a commercial product ready for production? What are the documentation do we consider, and prepare to have a successful design transfer?
The post is open for discussion, and their personal experience are highly appreciated.