Mary Mellows

Mary Mellows is a regulatory affairs professional with 20 years of extensive experience in the medical device industry. Currently serving as a Principal Regulatory Specialist at Hologic, Inc., Mary oversees FDA and European Union regulatory responsibilities for breast biopsy marker product lines. Previously, Mary held positions with Medtronic, where they managed global medical device registrations and developed regulatory strategies, and Covidien, where they progressed from Regulatory Associate to Senior Regulatory Specialist. In addition, Mary has a Bachelor of Arts in Psychology from the University of Vermont and a Master of Business Administration from the University of New Haven.