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Medical Program: The FAERS Public Dashboard and its Value to the Pharmaceutical Industry

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The FAERS Public Dashboard and its Value to the Pharmaceutical Industry

The FAERS Public Dashboard and its Value to the Pharmaceutical Industry
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    Hear the architects of the FAERS Public Dashboard share how this online tool is helping consumers transform raw data into usable information.
    • Overview

      The FDA has made strides in improving transparency and data access, and has implemented tools to allow the pharmaceutical industry and the public to transform raw data into usable information. One of these tools is called the FDA Adverse Event Reporting System (FAERS) Public Dashboard. In this episode, the architects of the FAERS Public Dashboard – Deputy Director of the Regulatory Science Staff Suranjan De, and Acting Team Lead in Regulatory Science Information Sanjay Sahoo—both of CDER’s Office of Surveillance and Epidemiology, highlight their work with this new online tool.

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