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Clinical Trial Data Sharing: A Framework for Success

The numerous stakeholders involved in clinical research (e.g., patients, volunteers, investigators, sponsors, patient advocacy groups) can all agree that data sharing is essential, but it’s hardly routine as a current part of the clinical trial lifecycle. To address the various challenges and barriers related to sharing of clinical trial data, the Institute of Medicine (IOM) was commissioned to assemble a committee to reviewStrategies for Responsible Sharing of Clinical Trial Data and identify guiding principles and framework for data sharing.1 The committee’s report builds upon the draft document released for public comment January 2014 and released in its final format January 2015. The Sponsors