Annette M. Zinn, J.D., Ph.D., is a regulatory attorney with over 25 years of regulatory experience in the medical device industry. Previously she was regulatory counsel at Cyberonics for 13 years and regulatory specialist at Intermedics, Inc. for 7 years. During her career she has overseen successful pre-market approval applications (PMA) to the U.S. Food and Drug Administration. She instructed LLM students in FDA law and regulations at the University of Houston, Bates College of Law. She has a law degree from South Texas College of Law and is licensed to practice in the State of Texas. She has both M.P.H. and Ph.D. degrees from the University of Texas Houston, School of Public Health, where her research included the effect of modernization laws on FDA/CMS approvals.
Current role
Director of Regulatory Affairs at TAIT & Associates
Director of Regulatory Affairs at Mazen Animal Health
Director of Regulatory Affairs at Kinevant Sciences
Director of Regulatory Affairs at Proteon Pharmaceuticals
Director of Regulatory Affairs at Adlai Nortye Biopharma