Daniel Root

Daniel Root is a seasoned regulatory affairs specialist with extensive experience in the medical device industry. Currently serving as a Senior Regulatory Affairs Specialist at Boston Scientific since August 2019, Daniel focuses on the registration of FDA and EU intravenous catheters and control unit power supplies, while leading new product development projects and managing the transition of medical devices to EU MDR. Prior experience includes a Senior Regulatory Affairs Specialist role at Merck KGaA from February 2014 to August 2019, where Daniel oversaw medical device registrations and product launches across multiple global partners in over 60 countries. Earlier, Daniel worked as a Regulatory Affairs Specialist at NCH Corporation, coordinating state business licenses for pesticide applications and managing state registrations. Daniel holds a Bachelor of Applied Science in Biology from Santa Clara University.