Guidance for industry acute bacterial sinusitis, developing drugs for treatment.Format: [electronic resource] :
Publisher: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research,
Date: [2007] This title can be found in 1 Iowa libraries.
Pharmaceutical law : regulation of research, development, and marketing /Publisher: Arlington, Va : BNA Books, BNA Books,
Date: c2007. This title can be found in 2 Iowa libraries.
Guidance for industry and review staff recommended approaches to integration of genetic toxicology study results.Format: [electronic resource] :
Publisher: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research,
Date: [2006] This title can be found in 1 Iowa libraries.
New drug development science, business, regulatory, and intellectual property issues cited as hampering drug development efforts : report to conggressional requesters.Format: [electronic resource] :
Publisher: [Washington, D.C.] : U.S. Government Accountability Office,
Date: [2006] This title can be found in 1 Iowa libraries.
Research and development in the pharmaceutical industry /Author: Austin, David H.
Publisher: Washington, D.C. : Congress of the United States, Congressional Budget Office,
Date: 2006. This title can be found in 1 Iowa libraries.
Pharmaceutical law, 2006 : across the product life cycle /Publisher: New York, N.Y. : Practising Law Institute,
Date: c2006. This title can be found in 2 Iowa libraries.
Pharmaceutical development phases a duration analysis /Format: [electronic resource] :
Author: Abrantes-Metz, Rosa M.
Publisher: Washington, DC : Bureau of Economics, Federal Trade Commission,
Date: [2004] This title can be found in 1 Iowa libraries.
FDA regulatory affairs : a guide for prescription drugs, medical devices, and biologics /Publisher: Boca Raton, FL : CRC Press,
Date: c2004. This title can be found in 1 Iowa libraries.
Guidance for industry bioanalytical method validation.Format: [electronic resource] :
Publisher: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research :
Date: [2001] This title can be found in 1 Iowa libraries.
Guidance for industry extended release oral dosage forms, development, evaluation, and application of in vitro/in vivo correlations.Format: [electronic resource] :
Publisher: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research.,
Date: [1997] This title can be found in 2 Iowa libraries.
SUPAC-IR questions and answers about SUPAC-IR guidanceFormat: [electronic resource].
Publisher: [Rockville, Md.] : Food and Drug Administration,
Date: [1997] This title can be found in 1 Iowa libraries.
Norplant and contraceptive pricing : conflict of interest, protection of public ownership in drug development deals between tax-exempt, federally supported labs and the pharmaceutical industry : hearing before the Subcommittee on Regulation, Business Opportunities, and Technology of the Committee on Small Business, House of Representatives, One Hundred Third Congress, first session.Publisher: Washington : For sale by the U.S. G.P.O., Supt. of Docs., Congressional Sales Office,
Date: 1994- This title can be found in 1 Iowa libraries.
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