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01867aam a2200361Ia 4500 001 7FE9DAB0FE5F11E2B6A414D3DAD10320 003 SILO 005 20130806010419 006 m d f 007 cr an||||||||| 008 090602s2008 mdu s f000 0 eng d 035 $a (OCoLC)368275510 040 $a GPO $c GPO $d MvI $d SILO 074 $a 0499-T (online) 086 0 $a HE 20.4702:R 26/4 245 00 $a Guidance for industry $h [electronic resource] : $b providing regulatory submissions in electronic format : human pharmaceutical product applications and related submissions using the eCTD specifications. 246 30 $a Providing regulatory submissions in electronic format 246 30 $a Human pharmaceutical product applications and related submissions using the eCTD specifications 260 $a Silver Spring, MD : $b U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research ; $c [2008] 300 $a ii, 16 p. : $b digital, PDF file. 538 $a Mode of access: Internet at the FDA web site. Address as of 6/2/09: http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/UCM072349.pdf ; current access is available via PURL. 500 $a Title from PDF title page (viewed on June 2, 2009). 500 $a "June 2008". 500 $a "Revision 2". 650 0 $a Electronic filing systems $x Government policy $z United States. 650 0 $a Drugs $x Government policy $x Government policy $z United States. 710 2 $a Center for Drug Evaluation and Research (U.S.) 710 2 $a Center for Biologics Evaluation and Research (U.S.) 856 40 $u http://purl.access.gpo.gov/GPO/LPS113315 941 $a 2 952 $l UPAX334 $d 20230104041620.0 952 $l USUX851 $d 20160824025904.0 956 $a http://locator.silo.lib.ia.us/search.cgi?index_0=id&term_0=7FE9DAB0FE5F11E2B6A414D3DAD10320Initiate Another SILO Locator Search