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Drug Information Journal|December 11, 1986
Statistical analyses of adverse event data from clinical trials. Special emphasis on serious eventsR T O'NeillAlcohol and Alcoholism (Oxford, Oxfordshire). Supplement|March 1, 1996
Voice of the victims--the key to consensus and support for alcoholism researchJ T O'NeillContemporary Clinical Trials|November 13, 2020
Reacting to crises: The COVID-19 impact on biostatistics/epidemiologyRobert T O'NeillStatistics in Medicine|December 1, 1988
On sample sizes to estimate the protective efficacy of a vaccineR T O'NeillControlled Clinical Trials|December 31, 1997
Secondary endpoints cannot be validly analyzed if the primary endpoint does not demonstrate clear statistical significanceR T O'NeillAmerican Journal of Epidemiology|July 1, 1984
Sample sizes for estimation of the odds ratio in unmatched case-control studiesR T O'NeillStatistics in Medicine|May 15, 1995
Statistical concepts in the planning and evaluation of drug safety from clinical trials in drug development: issues of international harmonizationR T O'NeillStatistics in Medicine|October 21, 2003
Sam Greenhouse: his contributions as a consultant to the Food and Drug AdministrationRobert T O'NeillPageof 39