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001 9910698900203321
005 20090814124613.0
035   $a(CKB)5470000002396859
035   $a(OCoLC)319714996
035   $a(EXLCZ)995470000002396859
100   $a20090430d2007      ua             0
101 0 $aeng
135   $auran|||||||||
181   $ctxt$2rdacontent
182   $cc$2rdamedia
183   $acr$2rdacarrier
200 00$aGuidance for industry$b[electronic resource] $eproviding regulatory submissions to the Center for Biologics Evaluation and Research (CBER) in electronic format, lot release protocols
210  1$aRockville, MD :$cU.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Biologics Evaluation and Research,$d[2007]
215   $ai, 6 pages $cdigital, PDF file
300   $aTitle from PDF title page (viewed on Apr. 30, 2009).
300   $aNo longer available via Internet.
300   $a"November 2007".
517   $aGuidance for industry 
606   $aBiologicals$xTesting
608   $aElectronic records.$2lcgft
615  0$aBiologicals$xTesting.
712 02$aCenter for Biologics Evaluation and Research (U.S.)
801  0$bGPO
801  1$bGPO
801  2$bGPO
906   $aBOOK
912   $a9910698900203321
996   $aGuidance for industry$93434577
997   $aUNINA