2012 has only just begun, but the US Congress, the Food and Drug Administration and several health care industries will soon be busy with ironing out the details of new user fee acts (UFAs) and the reauthorization of expiring UFAs, says the influential think tank American Action Forum.
Below, is a brief description of potential obstacles that each UFA may face set out by the AAF, which says it will continue to cover the upcoming Congressional hearings regarding user fees.
Medical Device User Fee Act III (MDUFA III)
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