54 records matched your query       

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001 802CB722FE5F11E2B6A414D3DAD10320
003 SILO
005 20130806010419
006 m        d f      
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008 090603s2007    mdu     s    f000 0 eng d
035    $a (OCoLC)369245702
040    $a GPO $c GPO $d MvI $d SILO
074    $a 0499-T (online)
086 0  $a HE 20.4702:R 26/5
245 00 $a Guidance for industry $h [electronic resource] : $b providing regulatory submissions in electronic format, receipt date.
246 30 $a Providing regulatory submissions in electronic format, receipt date
260    $a Rockville, MD : $b U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research : $c [2007]
300    $a 6 p. : $b digital, PDF file.
538    $a Mode of access: Internet at the FDA web site. Address as of 6/3/09: http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/UCM072385.pdf ; current access is available via PURL.
500    $a Title from PDF title page (viewed on June 3, 2009).
500    $a "Draft guidance".
500    $a "June 2007".
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.
650  0 $a Biologicals $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/LPS113402
941    $a 1
952    $l USUX851 $d 20160824025931.0
956    $a http://locator.silo.lib.ia.us/search.cgi?index_0=id&term_0=802CB722FE5F11E2B6A414D3DAD10320