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Home » US FDA hammered over user fee accountability
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US FDA hammered over user fee accountability

April 26, 2022
By Mari Serebrov
In the second of two hearings before the U.S. Senate Health, Education, Labor and Pensions Committee on the next iteration of the FDA drug and device user fee agreements, the focus was supposed to be on advancing regulation and innovation. But Ranking Member Richard Burr (R-N.C.) shifted the spotlight April 26 to accountability in his opening remarks and subsequent questioning.
BioWorld BioWorld MedTech Drugs Medical devices and technologies Regulatory U.S. FDA

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