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DIA And FDA To Host Two Important Critical Path Workshops
Date:7/25/2008

Challenges] will feature speakers/panelists such as Janet Woodcock, MD, Director, Center for Drug Evaluation and Research, FDA; Mark B. McClellan, MD, PhD, Chair, Reagan-Udall Foundation and Director, Engelberg Center for Health Care Reform Brookings; and Raymond Woosley, MD, PhD, President and CEO, Critical Path Institute.

The http://www.diahome.org/DIAHOME/Education/FindEducationalOffering.aspx?productID=17183&eventType=Meeting [Critical Path Transporter Workshop] will be held in collaboration with PhRMA, the American Association of Pharmaceutical Scientists, and International Society for the Study of Xenobiotics.

"Leading scientists from academia, the FDA, and industry will present and lead discussion on the current status of the rapidly emerging field of drug transporters, the clinical relevance of drug uptake and efflux transporters, and the application of in vitro and in vivo tools to drug discovery and development," notes Program Committee Member Shiew-Mei Huang, PhD, FCP, Deputy Director, Office of Clinical Pharmacology, CDER, FDA.

Featured sessions will include:

  • Focus on key transporters
  • Current and future technical challenges
  • Drug development and FDA examples

In March 2004, FDA first announced the Critical Path Initiative, which was designed to identify additional mechanisms through applied scientific studies to develop better methods and new technologies that may improve the product development process. Since that time, a number of efforts have launched to leverage collaborations to modernize development of new genomic, imaging, statistical, methodological, analytical, and informatics tools, with the ultimate goal of red
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