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NEW JERSEY CHAPTER

  • 2001 - 2005

     

past events



  • 2005 - program
    • Use of Advanced Computer Methods to Simplify the Analysis of Complex Clinical Drug Safety Data, Ana Szarfman et. al
    • Data Mining in the Real World: Five lessons learned in the pit, Richard D. De Veaux
    • Empirical Bayes Methods for Estimation of Adverse Event Rates in Clinical Trials and Active Surveillance, William DuMouchel
  • 2003
    • Advising the FDA: A Statistician’s Perspective, Stephen L George
    • Defining Success in Oncology Drug Development, Richard Pazdur
    • Using Bayesian Calculations to Address Clinical Trial Issues Directly, A. Lawrence Gould
  • 2002
    • Flexible Sample Size: Is There a Free Lunch?, Chris Jennison and Bruce Turnbull
    • Symposium on Group Sequential Inference, Cyrus R. Mehta
    • Problems and issues in adaptive clinical trial design, Gordon Lan
    • Inference and Operational Conduct Issues with Sample Size Adjustment Based On Interim Observed Effect Size, James Hung et. al
    • Self-Designing Trials: Further Thoughts and Advances, Lloyd D. Fisher
  • 2001
    • Developing e-Standards for Clinical Trials Data and Analyses, Steve Wilson
    • An Update on Statistical Issues Associated with the ICH, Robert O’Neill

 

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