Cynthia Fink, MPH, RAC
Cynthia is an experienced regulatory professional whose expertise includes developing and implementing regulatory strategies for pharmaceuticals and medical devices, designing clinical study programs and protocols, analyzing clinical study data, designing case report forms, designing and overseeing clinical and adverse event data management programs, preparing clinical study reports, and reviewing clinical data for regulatory submission suitability. She provides overall support for the preparation of regulatory submissions for drugs, biologics, and medical devices. She is also expert in identifying, analyzing, and interpreting clinical and epidemiological studies to assess relationships between risk factors or exposure to healthcare products and disease. Cynthia has a M.P.H. in Epidemiology and Biostatistics from the George Washington University School of Public Health and Health Services and a B.S.E in Biomedical Engineering from the Duke University School of Engineering. She maintains Regulatory Affairs Certification (RAC) from the Regulatory Affairs Professional Society (RAPS).