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Shaping Best Practices For Standardized Medical Imaging In Clinical Trials
Date:8/26/2008

sement of a rigorously defined metrics that quantify the quality of imaging enterprises in biopharmaceutical development;
  • An explanation of the issues surrounding the quantification of adjudication rates across therapeutic areas and imaging technologies;

  • Harmonization of imaging as a quantitative measure of drug-induced changes in multi-center clinical trials; and

  • The adoption of a standard, open-source, internet-based application for transferring data from sites of acquisition to central repositories.
"Working alongside experts from academia, professional imaging societies, non-profit consortia, and governmental agencies, meeting attendees will help to shape best practices for standardized medical imaging in clinical trials," notes Program Chair P. David Mozley, MD, Senior Director, Imaging, Merck Research Laboratories.

About the http://www.diahome.org/ [Drug Information Association (DIA)]
DIA serves more than 30,000 professionals in the biotechnology, pharmaceutical and regulatory industries worldwide. Through its domestic and international meetings, training courses, workshops and webinars, DIA provides a neutral global forum for the exchange of information critical to the advancement of the drug discovery and lifecycle management processes. Headquartered in Horsham, PA, USA, and with offices in Basel, Switzerland, Tokyo, Japan, and Mumbai, India, the Association is led by its volunteer-based Board of Directors and executive management team. For more information, visit

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