AR 184 – New JerseyStatus: Inactive / Dead
Year Introduced: 2017
URGES FDA TO EXPEDITE APPROVAL PROCESS FOR GENERIC DRUGS: To expedite access to generic drugs, for the next 47 reauthorization of the Generic Drug User Fee Act (GDUFA), the FDA should consider additional steps to improve ANDA review efficiency, so that the current backlog of pending applications and 2 the average time required to review generic drug applications can 3 be reduced.
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