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Jeannie Cecka
Independent Clinical and Regulatory Consultant
Jeannie Gifford is a Clinical and Regulatory executive with extensive experience in developing strategic approaches for gaining product approval of medical devices in the US and International markets.
With a strong background in working with the FDA, Jeannie excels at guiding start-up medical device companies in implementing regulatory and clinical plans to achieve their goals.
As a strategic thinker and negotiator, she showcases excellent project management skills in uniting teams towards conducting scientifically sound clinical trials leading to successful product approvals.
Jeannie's specialties cover a diverse array of medical devices, including Ophthalmology, Cardiovascular, Neurosurgery, Imaging, Lasers and RF, Plastic and General Surgery, Blood Glucose Monitoring.
Her educational background includes a Master of Business Administration from Pepperdine University, The George L. Graziadio School of Business and Management, and a Bachelor of Science in Biology from the University of California, Irvine.
With a rich professional history, Jeannie has served in various roles such as Independent Clinical and Regulatory Consultant at Cecka Consulting Group, Vice President of Regulatory and Clinical Affairs at Sunrise Technologies, Inc., and Director of Worldwide Clinical Research at Allergan, among others.
