AR 184 – New Jersey
Status: Inactive / DeadYear Introduced: 2017
Link: https://www.njleg.state.nj.us/2016/Bills/AR/184_I1.HTM
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.
Key Issues:
PHARMACEUTICALS
Biosimilar or Generic Competition
Return to Database Search
© 2018- The SLIHCQ Database. Initial funding for this project was provided by the Robert Wood Johnson Foundation. The views expressed here do not necessarily reflect the views of the Foundation.
Associated Litigation:
No items found
Leave A Comment