Edward “Ted” Sherwood

Director, Office of Regulatory Operations (ORO), OGD, CDER

Ted Sherwood has been the Director of the Office of Regulatory Operations (ORO) within the Office of Generic Drugs (OGD) since 2014.  ORO consists of three divisions: Division of Project Management, Division of Filing Review, and Division of Labeling Review. Previously, he served as the Associate Director of Immediate Office Operations, Office of Pharmaceutical Science [now the Office of Pharmaceutical Quality (OPQ)].  Prior to joining OPQ in 1999, he spent a dozen years in OGD.  He held various positions including, reviewing new submissions for determination of fileability, conducting program analyses, and coordinating congressional activities.  Ted received his bachelor’s degree from the University of Maryland in 1992.

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