The Animal Drug User Fee Act (ADUFA) and the Animal Generic Drug user Fee Act (AGDUFA) authorize FDA to collect fees for animal drug applications. These fees provide funding for increased review staff, training and development for staff members, and for refining business processes and developing policies targeted at more efficient review.
Page Last Updated: 06/26/2014
Note: If you need help accessing information in different file formats, see Instructions for Downloading Viewers and Players.
Language Assistance Available: Español | 繁體中文 | Tiếng Việt | 한국어 | Tagalog | Русский | العربية | Kreyòl Ayisyen | Français | Polski | Português | Italiano | Deutsch | 日本語 | فارسی | English