01541oam 2200421Ia 450 991069813910332120100112152118.0(CKB)5470000002395591(OCoLC)316342011(EXLCZ)99547000000239559120090319d2009 ua 0engurbn|||||||||txtrdacontentcrdamediacrrdacarrierGuidance for industry[electronic resource] clinical pharmacology section of labeling for human prescription drug and biological products : content and formatRockville, MD :U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER) :Center for Biologics Evaluation and Research (CBER),[2009]11 pages digital, PDF fileTitle from title screen (viewed on Mar. 19, 2009)."Draft guidance.""February 2009."Guidance for industry DrugsLabelingUnited StatesBiological productsLabelingUnited StatesDrugsLabelingBiological productsLabelingCenter for Drug Evaluation and Research (U.S.)Center for Biologics Evaluation and Research (U.S.)GPOGPOGPOCDSGPOBOOK9910698139103321Guidance for industry3434577UNINA