The third iteration of the Generic Drug User Fee Amendments should allocate more funding for overseas FDA inspections and postmarket surveillance because the quality of generic drugs has a direct effect on the U.S. drug supply chain and patient safety, regulatory experts told a panel of FDA officials on Tuesday (July 21). Kaiser Permanente’s senior vice president of government relations, Anthony Barrueta, said ensuring product quality and a stronger supply chain should be high priorities for the next round of...