AVMA President Dr. Lori Teller testified before the House Energy and Commerce Subcommittee on Health on March 30, 2023. She discussed the importance of reauthorizing the Animal Drug User Fee Act (ADUFA) and the Animal Generic Drug User Fee Act (AGDUFA). The legislation is up for reauthorization every five years and is critical to ensuring a predictable pathway to market for new and innovative animal drugs and generic animal drugs.
The AVMA supports the collection and effective utilization of user fees to enhance the U.S. Food and Drug Administration Center for Veterinary Medicine’s (FDA CVM) review and approval of pioneer and generic animal drugs. Throughout 2022, the AVMA provided verbal and written comments to the FDA CVM regarding the needs of veterinarians in the reauthorization of these programs.
“Veterinarians need additional new, innovative, and generic animal drugs that have been demonstrated to be safe and effective to help protect animal and public health,” said Teller. “We support the collection of user fees for new and generic animal drug applications when they are used to expedite the review and approval process for these products.”
Past animal drug user fee agreements have advocated for improved efficiency of the animal drug review and approval process; however, more can be done. The AVMA supports:
About the AVMA
Serving more than 100,000 member veterinarians, the AVMA is the nation's leading representative of the veterinary profession, dedicated to improving the health and wellbeing of animals, humans and the environment. Founded in 1863 and with members in every U.S. state and territory and more than 60 countries, the AVMA is one of the largest veterinary medical organizations in the world. Informed by our members' unique scientific training and clinical knowledge, the AVMA supports the crucial work of veterinarians and advocates for policies that advance the practice of veterinary medicine and improve animal and human health.
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