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  1. FDA-TRACK: Agency-wide Program Performance

FDA-TRACK: Combination Products Performance Dashboards

 

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First enacted in 2012 as part of the Food and Drug Administration Safety and Innovation Act (FDASIA), the FDA User Fee Reauthorization Act of 2022, reauthorizes FDA to assess and collect fees for generic drug products from October 2023 through September 2027. GDUFA is designed to speed the delivery of safe and effective generic drugs to the public and improve upon the predictability of the review process.

The Office of Combination Products Performance Dashboards (OCP Dashboards) provide a concise, interactive, and visual presentation of data presented in the legislatively mandated OCP Performance Report to Congress (the Report) as required by the Medical Device User Fee and Modernization Act of 2002. The OCP Dashboards are not intended to replace the Report and are to be used as a supplemental tool for viewing the data. 

 

Data Dashboards to be added.

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