Loading…
Attending this event?
avatar for Paul Brown

Paul Brown

FDA, United States
Associate Director for Pharmacology and Toxicology, OND, CDER
Dr. Brown's responsibilities include development and implementation of guidance and policy related to the nonclinical assessment of human pharmaceuticals. He has been at the FDA since 1996 when he joined the Division of Dermatology and Dental Drug Products as a Pharmacology/Toxicology reviewer. He was supervisor for Pharmacology/Toxicology in this Division from 2003 to 2008. Prior to coming to the FDA he was a Pharmacology Research and Training Fellow in the National Cancer Institute from 1991 to 1996. He worked on multidrug resistance gene structure and function in the Laboratory of Experimental Carcinogenesis. He received his Ph.D. in toxicology from the University of Maryland in 1991.

My Speakers Sessions

Monday, June 17
 

3:30pm PDT

#150: Building Trust in New Alternative Methods in Investigational New Drug Applications Room 1AB
 
Share Modal

Share this link via

Or copy link