SciLucent’s staff includes scientific, medical, and regulatory professionals with expertise and experience in all aspects of healthcare product development and marketed product support.
Cynthia A. Fink, M.P.H., RAC
Clinical Program Development and Implementation; Regulatory Strategy, Documentation, and Implementation
Cynthia Fink assists medical device, pharmaceutical, and biopharmaceutical companies with clinical and regulatory challenges. Cynthia's expertise includes developing and implementing regulatory strategies for medical devices and pharmaceuticals, 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 also provides statistical analysis and interpretation expertise for clinical and epidemiological studies. Cynthia's expertise includes orthopedic, cardiovascular, and plastic and reconstructive medical devices and cardiovascular, oncologic, immunologic, and anti-infective drugs and vaccines.
