The development of new drugs and medical devices follows well-established approval paths to make sure that they are safe when they reach the public. The U.S. FDA recommends five stages for the medical device and pharma development process, and some Asia Pacific countries' regulators suggest similar steps.
In this virtual hands-on workshop, Minitab Technical Services Manager Ming Dong will walk you through the Minitab Statistical Software and Minitab Workspace quality and visual tools that can be used in each stage. He will also take you through the common challenges faced by pharmaceutical and medical device manufacturers.