Dan Davis

Dan Davis is an experienced Global Regulatory Affairs leader currently serving as Associate Director at Baxter International Inc., where they lead a global regulatory team in the development and registration of medical devices and combination products. Previously, Dan held various roles at Baxter Healthcare, including Senior Manager for U.S. Regulatory Affairs and Pipeline Portfolio Lead, overseeing regulatory strategies and submissions for Class II and Class III medical devices. Dan’s background also includes a Ph.D. candidacy and research at the University of Illinois at Chicago, where they focused on bioengineering, with a double focus on rehabilitation engineering and cellular and tissue engineering.