The regulatory environments are changing, particularly in Europe. In the next few years, we are expecting a complete overhaul of the regulatory standards practiced by the E.U. These events will dramatically change how (and where) medical device manufacturers think about product launches. In this webinar, Jon Speer of Greenlight Guru (Indianapolis) will explore the changing environment in the E.U. and provide some insight into what device companies should expect to see in the region. He will also discuss how it contrasts with U.S. FDA’s processes. Finally, he will offer some advice on the best regions to launch new products.