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Addressing the FDA's performance, efficiency, and use of resources : hearings of the Committee on Labor and Human Resources, United States Senate, One Hundred Fifth Congress, first session ... March 19 and April 11, 1997
by
United States. Congress. Senate. Committee on Labor and Human Resources
1997
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ASK AT REFERENCE DESK
21st century cures : modernizing clinical trials : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Thirteenth Congress, second session, July 9, 2014
by
United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health
2015
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Innovation in clinical trial methodologies lessons learned during the Corona pandemic
2021
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FDA's drug and device review process : hearing before the Subcommittee on Oversight and Investigations of the Committee on Energy and Commerce, House of Representatives, One Hundred Second Congress, second session, February 6, 1992
by
United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Oversight and Investigations
1992
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Y 4.EN 2/3:102-132
FDA Reauthorization Act of 2017 (FDARA, P.L. 115-52)
by
Sarata, Amanda K.
2018
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Annual performance report, Prescription Drug User Fee Act of 1992 fiscal year : ... report to Congress
1995
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Guide for detecting fraud in bioresearch monitoring inspections
1993
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Book and Microform
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Joyner - Microforms B300
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HE 20.4008:F 86
Council on Competitiveness and FDA plans to alter the drug approval process at FDA : hearing before the Human Resources and Intergovernmental Relations Subcommittee of the Committee on Government Operations, House of Representatives, One Hundred Second Congress, second session, March 19, 1992
by
United States. Congress. House. Committee on Government Operations. Human Resources and Intergovernmental Relations Subcommittee
1993
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Y 4.G 74/7:C 83/3
Characterizing and communicating uncertainty in the assessment of benefits and risks of pharmaceutical products workshop summary
by
Caruso, Denise, 1956-
2014
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Challenges to FDA's ability to monitor and inspect foreign clinical trials
by
United States. Department of Health and Human Services. Office of Inspector General
2010
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