Ramona Lloyd

Biography

Ramona Lloyd, PhD, is Vice President, Regulatory Affairs and Quality at Optinose. In this role, Dr. Lloyd is responsible for regulatory strategy and quality in support of development and commercialization activities. A regulatory professional for more than 20 years, Dr. Lloyd has led or participated in the submission of numerous global investigational applications and successful marketing applications for small molecules, biologics and devices across multiple therapeutic areas. Prior to joining Optinose, she served as both a consultant to the pharmaceutical industry and as an executive with Sanofi-Aventis, Bristol Myers-Squibb and Johnson & Johnson. She acted as Senior Vice President of Regulatory Affairs and Safety for ImClone Systems and has served as Vice President of Regulatory Affairs and Quality for public and private biotechs, leading global regulatory strategy, regulatory submissions through product approval and key meetings with global regulatory authorities. Dr. Lloyd earned a doctorate in molecular genetics and microbiology from Robert Wood Johnson Medical School at Rutgers University and was a researcher at the Center for Advanced Biotechnology and Medicine. She also earned a Regulatory Affairs Certification (RAC), the professional credential in regulation of healthcare products

Research Interest

Business