side effects
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FDA Wants To Use EMRs To Streamline Adverse Drug Event Reporting
Ashley Gold | FierceEMR | January 8, 2014
The U.S. Food and Drug Administration wants to leverage electronic medical records to probe for adverse drug events, according to a recent article in Regulatory Focus. Big data has the power to help expose adverse events more quickly than ever, and the FDA wants to use that to assess drug side effects. Read More »
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