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  1. 1
    Medical Devices Technical Corrections Act : report (to accompany S. 1881) (including cost estimate of the Congressional Budget Office).
    Published 2004
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  2. 2
    Medical Device User Fee Stabilization Act of 2005 : report, together with additional views (to accompany S. 1420).
    Published 2005
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  3. 3
    The FDA medical device user fee program : MDUFA IV reauthorization /
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  4. 4
    An Act to Amend the Federal Food, Drug, and Cosmetic Act to Revise and Extend the User-Fee Programs for Prescription Drugs, Medical Devices, Generic Drugs, and Biosimilar Biological Products, and for Other Purposes.
    Published 2017
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  5. 5
    Medical Device User Fee and Modernization Act (MDUFMA) reauthorization /
    by Williams, Erin D.
    Published 2019
    Available to Lehigh users via MARCIVE
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  6. 6
    Examining FDA's Medical Device User Fee Program : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Fifteenth Congress, first session, March 28, 2017.
    Published 2018
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  7. 7
    Food and Drug Administration methodologies for identifying and allocating costs of reviewing medical device applications are consistent with federal cost accounting standards, and staffing levels for reviews have generally increased in recent years.
    by Martin, Robert E.
    Published 2007
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  8. 8
    Food and Drug Administration revenue information on certain companies participating in the Medical Device User Fee Program.
    by Williamson, Randall B.
    Published 2007
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  9. 9
    FDA user fees and the regulation of drugs, biologics, and devices : comparative analysis of S. 3187 and H.R. 5651 /
    by Thaul, Susan
    Published 2018
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  10. 10
    Medical Device User Fee and Modernization Act of 2002 : supplemental report (to accompany H.R. 3580).
    Published 2002
    Pt. 2, text version:
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