Prescription Drug User Fee Act (PDUFA)
This year marks the sixth reauthorization of the Prescription Drug User Fee Act (PDUFA). The user fee program was created to authorize the Food and Drug Administration (FDA) to collect user fees from biopharmaceutical companies to supplement its funding and review and approve innovative products faster and more efficiently. Thanks to PDUFA, the United States is the world leader in the development of biomedical products.
New Jersey Congressional staff recently participated in a briefing to learn more about why it is critical for Congress to pass the PDUFAVII reauthorization proposal which was submitted to Congress on January 12, 2022.
Learn more about PDUFA here: