FDA Commissioner Robert Califf told lawmakers he’s ready to work with them to bring more drug manufacturing to the US and laid out the agency’s progress to ramp up overseas inspections at a congressional hearing Thursday.
Appearing before a House Appropriations panel to defend the agency’s budget request for fiscal year 2025, representatives peppered Califf with questions about how the FDA can play a role in reshoring overseas generic drug manufacturing to the US. He also told the panel that while challenging, the FDA has made some progress in conducting more unannounced inspections overseas.
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