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212 Books found.
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| 1. |
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New Drug Development: A Regulatory Overview
by Mark Mathieu, Parexel International Corporation, Anne G. Evans
Hardcover,
Parexel Intl Corp
(May 2005)
Other Formats:
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Book |
Hardcover |
List Price: $145.00
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| 2. |
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Inside The FDA: The Business And Politics Behind The Drugs We Take And The Food We Eat
by Fran Hawthorne, Dr. A
Hardcover,
John Wiley & Sons Inc
(February 2005)
List Price: $27.95
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Development of Fda-Regulated Medical Products: Prescription Drugs, Biologics, and Medical Devices
by Elaine Whitmore
Hardcover,
Asq Pr
(December 2003)
List Price: $50.00
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Protecting America's Health: The Fda, Business, and One Hundred Years of Regulation
by Philip J. Hilts
Paperback,
Univ of North Carolina Pr
(September 2004)
Other Formats:
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List Price: $19.95
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Drug User Fees: Enhancing Patient Access and Drug Safety Hearing of the Committee on Health, Education, Labor, and Pensions, United States Senate, One Hundred Tenth Congress, First Session, on Examining Enhancing Patient Access and Drug Safety Relating to Prescription
by United States
Book,
U.S. G.P.O.
(January 2008)
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Agriculture, Rural Development, Food and Drug Administration, and Related Agencies Appropriations for 1997: Hearings before a Subcommittee of the Committee on Appropriations, House of Representatives, One Hundred Third Congress, Second Session
by United States
Book,
U.S. G.P.O.
(January 1996)
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Omega 3 Fatty Acids
by Robert P. Harris
Paperback,
Novinka Books
(January 2006)
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The Need for FDA Regulatory Reform to Protect the Health and Safety of Americans: Hearing before the Subcommittee on National Economic Growth, Natural Resources, and Regulatory Affairs of the Committee on Government Reform and Oversight, House of Representatives, One Hundred Fourth Congress, First Session, June 9, 1995
by United States
Book,
U.S. G.P.O.
(January 1996)
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Role of Commissioner of Food and Drugs: Hearing before the Committee on Labor and Human Resources, United States Senate, One Hundred Second Congress, First Session, on Examining the Role of the Current Commissioner of the Food and Drug Administration, March 6, 1991
by United States
Book,
U.S. G.P.O.
(January 1992)
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FDA's Generic Drug Enforcement and Approval Process: Hearings before the Subcommittee on Oversight and Investigations of the Committee on Energy and Commerce, House of Representatives, One Hundred Second Congress, First Session, March 7 and June 5, 1991
by United States
Book,
U.S. G.P.O.
(January 1992)
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