01448nam 2200373Ia 450 991069872380332120090423145500.0(CKB)5470000002396620(OCoLC)319069332(EXLCZ)99547000000239662020090423d2008 ua 0enguran|||||||||txtrdacontentcrdamediacrrdacarrierGuidance for industry[electronic resource] providing regulatory submissions in electronic format : human pharmaceutical product applications and related submissions using the eCTD specificationsSilver Spring, MD :U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research ;Rockville, MD :Center for Biologics Evaluation and Research,[2008]ii, 16 pages digital, PDF fileTitle from PDF title page (viewed on Apr. 23, 2009)."June 2008.""Revision 2."Guidance for industry Drug approvalUnited StatesElectronic filing systemsUnited StatesDrug approvalElectronic filing systemsCenter for Biologics Evaluation and Research (U.S.)GPOGPOBOOK9910698723803321Guidance for industry3434577UNINA