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Optimizing the Transition from Preclinical to Clinical Research
Program Code:
269
Date:
Tuesday, June 25, 2013
Time:
4:00 PM to 5:30 PM
EST
CHAIR
:
Stella Stergiopoulos,
(SCHSUP), Project Manager,
Tufts Center for the Study of Drug Development, United States
Stella Stergiopoulos manages multi-sponsored and grant funded research projects at Tufts CSDD. She has experience conducting research on pharmaceutical industry practices and trends affecting pharmaceutical outsourcing practices, duration metrics, resource management, and protocol design.
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SPEAKER
(S):
Stella Stergiopoulos,
(SPKSUP), Project Manager,
Tufts Center for the Study of Drug Development, United States
Stella Stergiopoulos manages multi-sponsored and grant funded research projects at Tufts CSDD. She has experience conducting research on pharmaceutical industry practices and trends affecting pharmaceutical outsourcing practices, duration metrics, resource management, and protocol design.
|
Laszlo Urban,
MD,PhD (SPKNON), Head, Preclinical Safety Profiling,
Novartis Institutes for Biomedical Research, United States
Laszlo Urban, MD, PhD: Global Head of Preclinical Safety Profiling at NIBR. Developed early in vitro safety profile program that provides general access to integrated information. Published +140 articles, book chapters & patents, edited 3 books & served on the editorial board of several journals.
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Simone Braggio, DrSc (SPKNON), Director, Drug Design and Discovery, Aptuit, Italy
Description
This session will highlight strategies for transitioning from nonclinical to early phase drug discovery most efficiently. The first presentation will discuss current industry processes and perceived costs in preclinical and early phase drug development. The second presentation will focus on risk mitigation in early phase studies, while the third presentation will focus on strategies for bridging the gap between preclinical and clinical development.