Month: November 2017

Clean Room Manufacturing

How to Create an Easy Transition From the Validation Process to Manufacturing

One of the most important phases of a medical product development life cycle is the relationship between your company‚Äôs validation expert and the original equipment manufacturer (OEM) of your medical product. It is the test run for approval and commercialization. The importance of the transition from validation process to manufacturing will determine FDA approval, the… Read more »