U.S. flag An official website of the United States government
  1. Home
  2. About FDA
  3. Transparency
  4. FDA-TRACK: Agency-wide Program Performance
  5. FDA-TRACK: ADUFA Performance
  1. FDA-TRACK: Agency-wide Program Performance

FDA-TRACK: ADUFA Performance

Subscribe now!

Interested in receiving FDA-TRACK updates in your inbox?

On August 14, 2018, the third reauthorization of the Animal Drug User Fee Act (ADUFA), referred to as ADUFA IV, was signed into law. ADUFA amends the Federal Food, Drug, and Cosmetic Act (FD&C Act) by reauthorizing ADUFA for an additional five years (FY 2019 through FY 2023). ADUFA provides FDA with revenue to enhance the performance and predictability in review times for the animal drug industry and provides FDA with resources to improve its review of applications for new animal drugs, with the result that safe and effective new products will be more readily available. 

The Animal Drug User Fee Performance Dashboards (ADUFA Dashboards) provide a concise, interactive, and visual presentation of data presented in the legislatively mandated FY 2021 ADUFA Performance Report to Congress for the Animal Drug User Fee Act (the Report). The ADUFA Dashboards are not intended to replace the Report and are to be used as a supplemental tool for viewing the data. The ADUFA Dashboards reflect performance on submissions received and actions taken as of September 30, 2021. The ADUFA Dashboards present final performance in meeting ADUFA goals for FY 2020 and preliminary performance for FY 2021. Final ADUFA performance data for FY 2021 will be presented in the FY 2022 ADUFA Report and referenced in updated versions of the ADUFA Dashboards.

ADUFA Performance Dashboard User Guide

icon of a checklist next to a pencil

Animal Drug Applications and Supplements

The Animal Drug Applications and Supplements Dashboard displays current performance relating to the review of:

  • Original New Animal Drug Applications (NADAs) and Reactivations
  • Administrative NADAs
  • Non-Manufacturing Supplemental NADAs and Reactivations
  • Manufacturing Supplemental NADAs and Reactivations
  • Labeling Supplements
  • Investigational New Animal Drug (INAD) Study Submissions
  • INAD Protocol Submissions
  • Presubmission Conference
  • Tissue Residue Method Demonstrations

For historical performance goals, please see the Historical Performance: Animal Drug Applications and Supplements Dashboard.

Relevant Links

Sign up to receive FDA-TRACK updates

Get regular FDA email updates delivered on this topic to your inbox.

Back to Top