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Dr. Leona Saunders has a wealth of experience developing and implementing regulatory strategies for pharmaceutical, biotech, and medical device companies. With over two decades of experience, she has made significant contributions to the planning, execution, and submission of various regulatory applications.

Dr. Saunders' expertise extends to writing and editing clinical and nonclinical documentation and serving as the lead regulatory author on multiple programs for submissions to FDA and various international regulatory authorities. Dr. Saunders' academic qualifications include a Doctorate in Law and Public Policy, a Master's degree in Regulatory Affairs, and a Bachelor's degree in Leadership in Bioscience, all from Northeastern University. She also holds a Master's degree in Public Health from Florida International University. Her extensive educational background has given her a strong foundation in the legal, policy, and scientific aspects of regulatory affairs, enabling her to offer a comprehensive approach to regulatory strategy.