Livres sur le sujet « FOOD AND DRUGS ADMINISTRATION »
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O'Reilly, James T. Food and drug administration. 2e éd. [Eagan, MN] : Thomson/West, 2005.
Trouver le texte intégralO'Reilly, James T. Food and drug administration. 2e éd. [St. Paul, Minn.] : Thomson/West, 2005.
Trouver le texte intégralO'Reilly, James T. Food and drug administration. 2e éd. Colorado Springs, Colo : Shepard's/McGraw-Hill, 1993.
Trouver le texte intégralThe Food and Drug Administration. New York, N.Y : Chelsea House, 1988.
Trouver le texte intégralA, Rettig Richard, Earley Laurence E, Merrill Richard A et Institute of Medicine (U.S.). Division of Health Sciences Policy., dir. Food and Drug Administration advisory committees. Washington, D.C : National Academy Press, 1992.
Trouver le texte intégralCenter for Drug Evaluation and Research (U.S.), dir. Drugs@FDA. Washington D.C : U.S. Food and Drug Administration, Center for Drug and Evaluation Research, 2004.
Trouver le texte intégralBuchta, Teresa M. Food and Drug Administration, Cincinnati, Ohio. [Atlanta, Ga.?] : U.S. Dept. of Health and Human Services, Public Health Service, Centers for Disease Control and Prevention, National Institute for Occupational Safety and Health, 1992.
Trouver le texte intégralUnited States. Food and Drug Administration. Cincinnati District Office et National Institute for Occupational Safety and Health, dir. Food and Drug Administration, Cincinnati, Ohio. [Atlanta, Ga.?] : U.S. Dept. of Health and Human Services, Public Health Service, Centers for Disease Control and Prevention, National Institute for Occupational Safety and Health, 1992.
Trouver le texte intégralBuchta, Teresa M. Food and Drug Administration, Cincinnati, Ohio. [Atlanta, Ga.?] : U.S. Dept. of Health and Human Services, Public Health Service, Centers for Disease Control and Prevention, National Institute for Occupational Safety and Health, 1992.
Trouver le texte intégralPhilipson, Tomas J. Is the Food and Drug Administration safe and effective ? Cambridge, Mass : National Bureau of Economic Research, 2007.
Trouver le texte intégralACG, McLaughlin Margaret, et Library of Congress. Congressional Research Service, dir. Drug approval : Access to experimental drugs for severely ill patients. [Washington, D.C.] : Congressional Research Service, Library of Congress, 1989.
Trouver le texte intégral1942-, Cooper Richard M., et Food and Drug Law Institute (U.S.), dir. Food and drug law. Washington, D.C : Food and Drug Law Institute, 1991.
Trouver le texte intégralCeccoli, Stephen J. Pill politics : Drugs and the FDA. Boulder, Colo : Lynne Rienner Publishers, 2004.
Trouver le texte intégralUnited States. Food and Drug Administration, dir. Public Health Service : Food and Drug Administration. [Rockville, Md : Food and Drug Administration, 1988.
Trouver le texte intégralUnited States. Food and Drug Administration. History Office, dir. A guide to resources on the history of the Food and Drug Administration. Rockville, Md. (5600 Fishers Lane, Rockville 20857) : Food and Drug Administration, History Office, 1995.
Trouver le texte intégralFDA administrative enforcement manual. Boca Raton, FL : Taylor & Francis, 2005.
Trouver le texte intégral1942-, Wallace Robert B., et Oria Maria, dir. Enhancing food safety : The role of the Food and Drug Administration. Washington, D.C : National Academies Press, 2010.
Trouver le texte intégralFood and Drug Law Institute (U.S.), dir. Food and drug law and regulation. Washington, D.C : FDLI, 2008.
Trouver le texte intégralUS GOVERNMENT. Food and Drug Administration Modernization Act of 1997. [Washington, D.C. ? : U.S. G.P.O., 1997.
Trouver le texte intégralYorke, Jeffrey. FDA ensures equivalence of generic drugs. [Rockville, MD] (5600 Fishers Lane, Rockville 20857) : [Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Office of Public Affairs, 1993.
Trouver le texte intégralYorke, Jeffrey. FDA ensures equivalence of generic drugs. [Rockville, MD] (5600 Fishers Lane, Rockville 20857) : [Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Office of Public Affairs, 1993.
Trouver le texte intégralPure food : Securing the Federal Food and Drugs Act of 1906. Princeton, N.J : Princeton University Press, 1989.
Trouver le texte intégralUnited States. Food and Drug Administration. Requirements of laws and regulations enforced by the U.S. Food and Drug Administration. Rockville, MD : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, 1989.
Trouver le texte intégralUS GOVERNMENT. Compilation of laws enforced by the U.S. Food and Drug Administration and related statutes. Rockville, MD : The Administration, 1996.
Trouver le texte intégralUnited States. Food and Drug Administration. Food and Drug Administration Modernization Act of 1997 : FDA plan for statutory compliance. [Rockville, Md.] : FDA, 1998.
Trouver le texte intégralAdministration, United States Food and Drug. Food and Drug Administration Modernization Act of 1997 : FDA plan for statutory compliance. [Rockville, Md.] : FDA, 1998.
Trouver le texte intégralUnited States. Food and Drug Administration. Food and Drug Administration Modernization Act of 1997 : FDA plan for statutory compliance. [Rockville, Md.] : FDA, 1998.
Trouver le texte intégralUnited States. Food and Drug Administration. Office of Public Affairs., dir. FDA-approved bargain drugs : Generic products must meet high standards. 2e éd. Rockville, MD : Dept. of Health and Human Services, Food and Drug Administration, Office of Public Affairs, 2003.
Trouver le texte intégralThe Food and Drug Administration's critical mission and challenges for the future : Hearing before the Committee on Oversight and Government Reform, House of Representatives, One Hundred Tenth Congress, first session, May 1, 2007. Washington : U.S. G.P.O., 2007.
Trouver le texte intégralUnited States. Food and Drug Administration. Office of Public Affairs., dir. FDA and the drug development process : How the agency ensures that drugs are safe and effective. Rockville, MD : Dept. of Health and Human Services, Food and Drug Administration, Office of Public Affairs, 2002.
Trouver le texte intégralOperations, United States Congress House Committee on Government. Human food safety and the regulation of animal drugs : Twenty-seventh report. Washington : U.S. G.P.O., 1986.
Trouver le texte intégralUnited States. Congress. House. Committee on Government Operations. Human food safety and the regulation of animal drugs : Twenty-seventh report. Washington : U.S. G.P.O., 1986.
Trouver le texte intégralUnited States. Congress. House. Committee on Government Operations. Human food safety and the regulation of animal drugs : Twenty-seventh report. Washington : U.S. G.P.O., 1986.
Trouver le texte intégralClinton, Bill. Reinventing regulation of drugs and medical devices. [Washington, D.C.?] : National Performance Review, 1995.
Trouver le texte intégralClinton, Bill. Reinventing regulation of drugs made from biotechnology. [Washington, D.C.?] : National Performance Review, 1995.
Trouver le texte intégralClinton, Bill. Reinventing regulation of drugs made from biotechnology. [Washington, D.C.?] : National Performance Review, 1995.
Trouver le texte intégral1948-, Gore Albert, et National Performance Review (U.S.), dir. Reinventing regulation of drugs and medical devices. [Washington, D.C.?] : National Performance Review, 1995.
Trouver le texte intégralClinton, Bill. Reinventing regulation of drugs and medical devices. [Washington, D.C.?] : National Performance Review, 1995.
Trouver le texte intégralClinton, Bill. Reinventing regulation of drugs and medical devices. [Washington, D.C.?] : National Performance Review, 1995.
Trouver le texte intégralInvestigations, United States Congress House Committee on Energy and Commerce Subcommittee on Oversight and. FDA's foreign drug inspection program : Weaknesses place Americans at risk : hearing before the Subcommittee on Oversight and Investigations of the Committee on Energy and Commerce, House of Representatives, One Hundred Tenth Congress, second session, April 22, 2008. Washington : U.S. G.P.O., 2008.
Trouver le texte intégralBuilding a 21st century FDA : Proposals to improve drug safety and innovation : hearing before the Committee on Health, Education, Labor, and Pensions, United States Senate, One Hundred Ninth Congress, second session, on examining proposals to improve drug safety and innovation, and S. 3807, to amend the Public Health Service Act and the Federal Food, Drug, and Cosmetic Act to improve drug safety and oversight, November 16, 2006. Washington : U.S. G.P.O., 2007.
Trouver le texte intégralUnited States. Congress. House. Committee on Energy and Commerce. Subcommittee on Oversight and Investigations. FDA's foreign drug inspection program : Weaknesses place Americans at risk : hearing before the Subcommittee on Oversight and Investigations of the Committee on Energy and Commerce, House of Representatives, One Hundred Tenth Congress, second session, April 22, 2008. Washington : U.S. G.P.O., 2008.
Trouver le texte intégralUnited States. Congress. House. Committee on Energy and Commerce. Subcommittee on Oversight and Investigations. FDA foreign drug inspection program : A system at risk : hearing before the Subcommittee on Oversight and Investigations of the Committee on Energy and Commerce, House of Representatives, One Hundred Tenth Congress, first session, November 1, 2007. Washington : U.S. G.P.O., 2008.
Trouver le texte intégralFDA foreign drug inspection program : A system at risk : hearing before the Subcommittee on Oversight and Investigations of the Committee on Energy and Commerce, House of Representatives, One Hundred Tenth Congress, first session, November 1, 2007. Washington : U.S. G.P.O., 2008.
Trouver le texte intégralFDA's foreign drug inspection program : Weaknesses place Americans at risk : hearing before the Subcommittee on Oversight and Investigations of the Committee on Energy and Commerce, House of Representatives, One Hundred Tenth Congress, second session, April 22, 2008. Washington : U.S. G.P.O., 2008.
Trouver le texte intégralUnited States. Congress. House. Committee on Government Operations. Human Resources and Intergovernmental Relations Subcommittee. FDA's regulation of the new drug Versed : Hearings before a subcommittee of the Committee on Government Operations, House of Representatives, One Hundredth Congress, second session, May 5 and 10, 1988. Washington : U.S. G.P.O., 1988.
Trouver le texte intégralUnited States. Public Health Service, dir. FDA drug bulletin April 1970 through October 1990 ; FDA medical bulletin March 1991 through June 1993 : Index by subject and title. Rockville, MD : Department of Health and Human Services, Public Health Service ; Food and Drug Administration, Office of Public Affairs, 1993.
Trouver le texte intégralD, Hynes Martin, dir. Preparing for FDA pre-approval inspections. New York : Marcel Dekker, 1999.
Trouver le texte intégralUnited States. Congress. House. Committee on Energy and Commerce. Subcommittee on Oversight and Investigations., dir. Filthy food, dubious drugs, and defective devices : The legacy of FDA's antiquated statute : a staff report. Washington : U.S. G.P.O., 1991.
Trouver le texte intégralUnited States. Food and Drug Administration. Food code : 1995 recommendations of the United States Public Health Service, Food and Drug Administration. Washington, D.C : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, 1995.
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