Carey Smoak
Carey successfully programmed /managed more than 20 regulatory submissions which have resulted in clearance/approval of FDA products – includes NDAs, BLAs, PMAs and 510(k)s. He has more than 35 years of SAS statistical programming experience and has more than 60 publications (peer reviewed journal articles, conference proceedings and abstracts) to his credit. Carey co-founded CDISC Medical Device team. The therapeutic areas of expertise include Thrombosis, In-vitro diagnostic screening and monitoring assays, Companion diagnostic assays, Vaccines, Alzheimer’s and other therapeutic areas!