Assessing User Fees Under the Generic Drug User Fee Amendments of 2017: Guidance for Industry
FDA has released this guidance to provide stakeholders with information regarding FDA’s implementation of the Generic Drug User Fee Amendments of 2017 (GDUFA II) under Title III of the FDA Reauthorization Act of 2017. Because GDUFA II created changes to the user fee program, this guidance serves to provide an explanation about the new fee structure and types of fees for which entities are responsible. This guidance describes the types of user fees authorized by GDUFA II, the process for submitting payments to FDA, the consequences for failing to pay generic drug user fees, and the process for requesting a reconsideration of a user fee assessment. This guidance also describes how FDA determines affiliation for purposes of assessing generic drug user fees. FDA will issue separate guidance documents regarding GDUFA II non-user fee requirements and processes.
Link to guidance document: https://www.fda.gov/downloads/
drugs/ guidancecomplianceregulatoryin formation/guidances/ucm582475. pdf
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