Donna-Bea Tillman, Ph.D Director, Office of Device Evaluation Center for Devices and Radiological Health Fostering Innovation on the Critical Path to Medical.
USFDA GUIDLINES
From Bench to the Clinic: Regulatory and Clinical Drug Development Strategies
Use of Outside Experts in FDAs Premarket Evaluation of Medical Devices Donna-Bea Tillman AU/OPM II AU/OPM II December 2004 An Action Learning Project Mans.
FDA Considerations For Regulation Of Nanomaterial Containing Products Nakissa Sadrieh, Ph.D. Office of Pharmaceutical Science, CDER, FDA.
1 LIVE INTERACTIVE LEARNING @ YOUR DESKTOP Tuesday, March 30, 2010 FDA/CFSAN: Food Safety & Globalization Adapting to a Changing Landscape Presented by:
