Tessa Yamut
VP Clinical/Regulatory Affairs & Quality Assurance
Business Management
Moximed
Italy
Biography
Ms. Yamut has more than 20 years of experience in the medical device industry. She specializes in getting start-up companies their regulatory/clinical approvals to either begin a clinical trial or commence a product commercial launch, domestically and internationally. Her experience includes authoring various FDA submissions, running clinical operations, and developing quality systems. Ms. Yamut also has extensive experience in gaining OUS approvals for clinical investigations and/or product launch in Europe, North America, South America, Australia, Asia, and Africa. Prior to joining Moximed, she has held several management positions at various start-up companies which include Vice President of Regulatory and Clinical Affairs at CHF Technologies and Cabochon Aesthetics (acquired by Ulthera), Sr. Director of Clinical and Regulatory Affairs at Spinal Kinetics and Relievant MedSystems, Director of Regulatory and Quality Affairs at Cardiovention, Inc., and Sr. Manager of Regulatory and Quality Affairs at Kyphon, Inc. (acquired by Medtronic) and General Surgical Innovations (acquired by Tyco Healthcare). Ms. Yamut studied Business Management and Administration at University of California and at Stanford Graduate School of Business.
Research Interest
Business Administration and Business Management
