Attending the 2015 RAPS Annual Conference? I will be a panelist at the New Pathways to Support Drug Development session on Monday at 11:00 am. Other expert panelists include: Elizabeth Ford, associate director of regulatory affairs, Office of Clinical Pharmacology, CDER, FDA; Xavier Luria, MD, senior consultant, drug development and regulation; and Sabine Haubenreisser, MSc, PhD, EMA liaison official at FDA. For more information on the session click here. Hope to see you there!
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