The FDA Medical Device User Fee Program

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Description

This report describes current law regarding medical device user fees, the impact of MDUFA on FDA review time of various medical device program budget, the MUDFA III proposal (legislative language and performance goals agreement), and issues that Congress is likely to take up as it works on the reauthorization of the medical device user fee program.

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37 p.

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Johnson, Judith A. April 24, 2012.

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This report is part of the collection entitled: Congressional Research Service Reports and was provided by the UNT Libraries Government Documents Department to the UNT Digital Library, a digital repository hosted by the UNT Libraries. It has been viewed 17 times. More information about this report can be viewed below.

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Description

This report describes current law regarding medical device user fees, the impact of MDUFA on FDA review time of various medical device program budget, the MUDFA III proposal (legislative language and performance goals agreement), and issues that Congress is likely to take up as it works on the reauthorization of the medical device user fee program.

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37 p.

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Congressional Research Service Reports

The Congressional Research Service (CRS) is the public policy research arm of Congress. This legislative branch agency works exclusively for Members of Congress, their committees and their staff. This collection includes CRS reports from the mid-1960's through 2018—covering a variety of topics from agriculture to foreign policy to welfare.

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Creation Date

  • April 24, 2012

Added to The UNT Digital Library

  • March 19, 2016, 1:57 p.m.

Description Last Updated

  • June 24, 2020, 3:13 p.m.

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Johnson, Judith A. The FDA Medical Device User Fee Program, report, April 24, 2012; Washington D.C.. (https://digital.library.unt.edu/ark:/67531/metadc812023/: accessed March 28, 2024), University of North Texas Libraries, UNT Digital Library, https://digital.library.unt.edu; crediting UNT Libraries Government Documents Department.

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