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O'Reilly, James T. Food and drug administration. Wyd. 2. [Eagan, MN]: Thomson/West, 2005.
Znajdź pełny tekst źródłaO'Reilly, James T. Food and drug administration. Wyd. 2. [St. Paul, Minn.]: Thomson/West, 2005.
Znajdź pełny tekst źródłaO'Reilly, James T. Food and drug administration. Wyd. 2. Colorado Springs, Colo: Shepard's/McGraw-Hill, 1993.
Znajdź pełny tekst źródłaThe Food and Drug Administration. New York, N.Y: Chelsea House, 1988.
Znajdź pełny tekst źródłaA, Rettig Richard, Earley Laurence E, Merrill Richard A i Institute of Medicine (U.S.). Division of Health Sciences Policy., red. Food and Drug Administration advisory committees. Washington, D.C: National Academy Press, 1992.
Znajdź pełny tekst źródłaCenter for Drug Evaluation and Research (U.S.), red. Drugs@FDA. Washington D.C: U.S. Food and Drug Administration, Center for Drug and Evaluation Research, 2004.
Znajdź pełny tekst źródłaBuchta, 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.
Znajdź pełny tekst źródłaUnited States. Food and Drug Administration. Cincinnati District Office i National Institute for Occupational Safety and Health, red. 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.
Znajdź pełny tekst źródłaBuchta, 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.
Znajdź pełny tekst źródłaPhilipson, Tomas J. Is the Food and Drug Administration safe and effective? Cambridge, Mass: National Bureau of Economic Research, 2007.
Znajdź pełny tekst źródłaACG, McLaughlin Margaret, i Library of Congress. Congressional Research Service, red. Drug approval: Access to experimental drugs for severely ill patients. [Washington, D.C.]: Congressional Research Service, Library of Congress, 1989.
Znajdź pełny tekst źródła1942-, Cooper Richard M., i Food and Drug Law Institute (U.S.), red. Food and drug law. Washington, D.C: Food and Drug Law Institute, 1991.
Znajdź pełny tekst źródłaCeccoli, Stephen J. Pill politics: Drugs and the FDA. Boulder, Colo: Lynne Rienner Publishers, 2004.
Znajdź pełny tekst źródłaUnited States. Food and Drug Administration, red. Public Health Service: Food and Drug Administration. [Rockville, Md: Food and Drug Administration, 1988.
Znajdź pełny tekst źródłaUnited States. Food and Drug Administration. History Office, red. 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.
Znajdź pełny tekst źródłaFDA administrative enforcement manual. Boca Raton, FL: Taylor & Francis, 2005.
Znajdź pełny tekst źródła1942-, Wallace Robert B., i Oria Maria, red. Enhancing food safety: The role of the Food and Drug Administration. Washington, D.C: National Academies Press, 2010.
Znajdź pełny tekst źródłaFood and Drug Law Institute (U.S.), red. Food and drug law and regulation. Washington, D.C: FDLI, 2008.
Znajdź pełny tekst źródłaUS GOVERNMENT. Food and Drug Administration Modernization Act of 1997. [Washington, D.C.?: U.S. G.P.O., 1997.
Znajdź pełny tekst źródłaYorke, 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.
Znajdź pełny tekst źródłaYorke, 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.
Znajdź pełny tekst źródłaPure food: Securing the Federal Food and Drugs Act of 1906. Princeton, N.J: Princeton University Press, 1989.
Znajdź pełny tekst źródłaUnited 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.
Znajdź pełny tekst źródłaUS GOVERNMENT. Compilation of laws enforced by the U.S. Food and Drug Administration and related statutes. Rockville, MD: The Administration, 1996.
Znajdź pełny tekst źródłaUnited States. Food and Drug Administration. Food and Drug Administration Modernization Act of 1997: FDA plan for statutory compliance. [Rockville, Md.]: FDA, 1998.
Znajdź pełny tekst źródłaAdministration, United States Food and Drug. Food and Drug Administration Modernization Act of 1997: FDA plan for statutory compliance. [Rockville, Md.]: FDA, 1998.
Znajdź pełny tekst źródłaUnited States. Food and Drug Administration. Food and Drug Administration Modernization Act of 1997: FDA plan for statutory compliance. [Rockville, Md.]: FDA, 1998.
Znajdź pełny tekst źródłaUnited States. Food and Drug Administration. Office of Public Affairs., red. FDA-approved bargain drugs: Generic products must meet high standards. Wyd. 2. Rockville, MD: Dept. of Health and Human Services, Food and Drug Administration, Office of Public Affairs, 2003.
Znajdź pełny tekst źródłaThe 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.
Znajdź pełny tekst źródłaUnited States. Food and Drug Administration. Office of Public Affairs., red. 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.
Znajdź pełny tekst źródłaOperations, 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.
Znajdź pełny tekst źródłaUnited 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.
Znajdź pełny tekst źródłaUnited 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.
Znajdź pełny tekst źródłaClinton, Bill. Reinventing regulation of drugs and medical devices. [Washington, D.C.?]: National Performance Review, 1995.
Znajdź pełny tekst źródłaClinton, Bill. Reinventing regulation of drugs made from biotechnology. [Washington, D.C.?]: National Performance Review, 1995.
Znajdź pełny tekst źródłaClinton, Bill. Reinventing regulation of drugs made from biotechnology. [Washington, D.C.?]: National Performance Review, 1995.
Znajdź pełny tekst źródła1948-, Gore Albert, i National Performance Review (U.S.), red. Reinventing regulation of drugs and medical devices. [Washington, D.C.?]: National Performance Review, 1995.
Znajdź pełny tekst źródłaClinton, Bill. Reinventing regulation of drugs and medical devices. [Washington, D.C.?]: National Performance Review, 1995.
Znajdź pełny tekst źródłaClinton, Bill. Reinventing regulation of drugs and medical devices. [Washington, D.C.?]: National Performance Review, 1995.
Znajdź pełny tekst źródłaInvestigations, 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.
Znajdź pełny tekst źródłaBuilding 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.
Znajdź pełny tekst źródłaUnited 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.
Znajdź pełny tekst źródłaUnited 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.
Znajdź pełny tekst źródłaFDA 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.
Znajdź pełny tekst źródłaFDA'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.
Znajdź pełny tekst źródłaUnited 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.
Znajdź pełny tekst źródłaUnited States. Public Health Service, red. 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.
Znajdź pełny tekst źródłaD, Hynes Martin, red. Preparing for FDA pre-approval inspections. New York: Marcel Dekker, 1999.
Znajdź pełny tekst źródłaUnited States. Congress. House. Committee on Energy and Commerce. Subcommittee on Oversight and Investigations., red. Filthy food, dubious drugs, and defective devices: The legacy of FDA's antiquated statute : a staff report. Washington: U.S. G.P.O., 1991.
Znajdź pełny tekst źródłaUnited 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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