Debbie Peacock

Debbie Peacock has extensive experience in regulatory affairs, specializing in medical devices and women's health products. Since April 2015, Debbie has served as a Senior Manager of Regulatory Affairs at Hologic, Inc., focusing on product submissions and support. Prior roles include Regulatory Affairs Manager at Covidien, where responsibilities included managing the electro surgical stapler line and overseeing product development in various markets, and at Fujifilm Medical Systems, where Debbie led teams on multiple regulatory submissions for medical imaging devices. Previous positions also include Regulatory Specialist at Siemens Medical Systems USA, with a focus on Class III submissions, and Regulatory Affairs Specialist at Teleflex Medical, contributing to technical file submissions for a left ventricle assist device. Debbie holds a Bachelor of Arts in English from the State University of New York College at Potsdam.