The US Food and Drug Administration has missed its 15 January deadline for submitting a plan to Congress on how much user fees the medical device industry should pay the agency to evaluate its products in fiscal years 2013-2017.
The FDA's current legislative authority for collecting user fees from companies under the Medical Device User Fee Act (MDUFA) ends in September 2012 and lawmakers will have to reauthorise the legislation for the agency to be able to continue collecting user fees (
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