Sep 9
Getz, the Executive Director at the Tufts Center for the Study of Drug Development (CSDD), presented findings from a study they did with TransCelerate BioPharma, which sheds light on the volume and purpose of data collected in clinical trial protocols. His talk centered on a fundamental paradox in modern clinical research: While we have an incentive to manage and optimize data collection, our protocols often accumulate an excessive amount of information that isn’t directly relevant to demonstrating the safety and efficacy of a drug.
Read the full article by Clinical Leader here.
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