Utilizing Electronic Health Record Data in Clinical Investigations

August 30, 2018


On July 19, 2018, the Food and Drug Administration (FDA) finalized its draft guidance for clinical trial sponsors, investigators, contract research organizations, institutional review boards and others using electronic health record (EHR) data in FDA-regulated clinical investigations.

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Garfunkel Wild can work with your organization to improve your clinical investigations processes through the use of electronic health data. For more information, please contact the Garfunkel Wild attorney with whom you usually work.