Showing 81 - 100 results of 111 for search '"Drug Approval United States"', query time: 0.22s Refine Results
  1. 81
    Report to industry.
    Published 1997
    Subjects: “...Drug Approval United States statistics....”
    Government Document Serial
  2. 82
    FDA user fees 2012 : issues related to accelerated approval, medical gas, antibiotic development, and downstream pharmaceutical supply chain : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Twelfth Congress, second session, March 8, 2012.
    Published 2013
    Subjects: “...Drug approval United States....”
    Get full text
    Get full text
    Government Document eBook
  3. 83
    FDA fast track and priority review programs /
    by Thaul, Susan
    Published 2018
    Subjects: “...Drug approval United States. http://id.loc.gov/authorities/subjects/sh2009123884...”
    Get full text
    Government Document Database
  4. 84
    FDA user fee agreements : improving medical product regulation and innovation for patients : hearing of the Committee on Health, Education, Labor, and Pensions, United States Senate, One Hundred Fifteenth Congress, first session on ... March 21, 2017.
    Published 2018
    Subjects: “...Drug approval United States....”
    Get full text
    Government Document eBook
  5. 85
    Purple Book Continuity Act of 2019 : report (to accompany H.R. 1520) (including cost estimate of the Congressional Budget Office).
    Published 2019
    Subjects: “...Drug approval United States....”
    PDF version
    Text version
    Government Document eBook
  6. 86
    FDA's authority to ensure that drugs prescribed to children are safe and effective /
    by Thaul, Susan
    Published 2019
    Subjects: “...Drug approval United States....”
    Get full text
    Government Document Database
  7. 87
    The CDER reference guide.
    Subjects: “...Drug Approval United States Directory....”
    Get full text
    Government Document Database
  8. 88
    Review of the proposed generic drug and biosimilars user fees and further examination of drug shortages : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Twelfth Congress, second session, February 9, 2012.
    Published 2013
    Subjects: “...Drug approval United States....”
    Get full text
    Get full text
    Government Document eBook
  9. 89
    Reviewing FDA's implementation of FDASIA : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Thirteenth Congress, first session, November 15, 2013.
    Published 2014
    Subjects: “...Drug approval United States....”
    Get full text
    Get full text
    Government Document eBook
  10. 90
    Unlocking hope : access to therapies for people with rare, progressive, and serious diseases : hearing before the Special Committee on Aging, United States Senate, One Hundred Eighteenth Congress, first session, Washington, DC, October 26, 2023.
    Published 2024
    Subjects: “...Drug approval United States....”
    Get full text
    Government Document eBook
  11. 91
    PDUFA V : medical innovation, jobs, and patients : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Twelfth Congress, first session, July 7, 2011.
    Published 2012
    Subjects: “...Drug approval United States. http://id.loc.gov/authorities/subjects/sh2009123884...”
    Electronic resource (PDF)
    Government Document eBook
  12. 92
    Reputation and power : organizational image and pharmaceutical regulation at the FDA /
    by Carpenter, Daniel P., 1967-
    Published 2010
    Subjects: “...Drug Approval United States....”
    Book
  13. 93
    The administration's FDA reforms and reduced biopharmaceutical drug prices /
    Published 2018
    Subjects: “...Drug approval United States....”
    Get full text
    Government Document eBook
  14. 94
    The impact of medical device and drug regulation on innovation, jobs, and patients : a local perspective : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Twelfth Congress, first session, September 26, 2011.
    Published 2012
    Subjects: “...Drug approval United States. http://id.loc.gov/authorities/subjects/sh2009123884...”
    Electronic resource (PDF)
    Government Document eBook
  15. 95
    Committee prints on administration legislative proposals on the Animal Drug User Fee Act Amendments of 2008 and the Animal Generic Drug User Fee Act of 2008 : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Tenth Congress, second session, June 5, 2008.
    Published 2008
    Subjects: “...Drug approval United States. http://id.loc.gov/authorities/subjects/sh2009123884...”
    Electronic resource (PDF)
    Government Document eBook
  16. 96
    FDA User Fee Agreements : Strengthening FDA and the Medical Products Industry for the Benefit of Patients.
    Published 2012
    Subjects: “...Drug approval United States. http://id.loc.gov/authorities/subjects/sh2009123884...”
    Electronic resource (PDF)
    Government Document eBook
  17. 97
    FDA User Fee Agreements : Improving Medical Product Regulation and Innovation for Patients.
    Published 2017
    Subjects: “...Drug approval United States. http://id.loc.gov/authorities/subjects/sh2009123884...”
    electronic resource (pdf)
    electronic resource (pdf)
    Government Document eBook
  18. 98
    The opioid epidemic and the Food and Drug Administration : legal authorities and recent agency action /
    by Staman, Jennifer A.
    Published 2018
    Subjects: “...Drug approval United States. http://id.loc.gov/authorities/subjects/sh2009123884...”
    Get full text
    Government Document Database
  19. 99
    Compassionate use and emergency use authorization for unapproved drugs : FDA policies and background /
    Published 2016
    Subjects: “...Drug approval United States. http://id.loc.gov/authorities/subjects/sh2009123884...”
    Connect to the full text of this electronic book
    eBook
  20. 100
    Perspectives of drug manufacturers : investigational new drug and new drug applications.
    Published 1990
    Subjects: “...Drug approval United States. http://id.loc.gov/authorities/subjects/sh2009123884...”
    Get full text
    Government Document eBook
Search Tools: RSS Feed – Email Search