Despite technological advances in clinical trials, current methods of detecting adverse events and patient outcomes in clinical trials have significant limitations. Patient provided information from clinic visits are often the only source of information for the detection and reporting of adverse events. Recall bias and missing medical records increases the chance of trial failure. This occurs not because the intervention is ineffective but because the efficacy of the intervention is less likely to be detectable statistically. Learn how to leverage new technologies to improve the detection and reporting of adverse events with this white paper.

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