Adverse Event Reviews: FDA Needs To Boost ‘Accuracy And Efficiency’

Agency seeks academic institutions and commercial organizations with tools that can conduct automated analysis of case reports from FAERS data.

FDA would like to cut back on the amount of time staffers have to spend poring over millions of adverse event case reports. To that end, the agency is looking for academic institutions or commercial organizations with technology that can run an automated analysis of the data.

FDA posted

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