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001 9910698834903321
005 20091119122230.0
035   $a(CKB)5470000002397518
035   $a(OCoLC)351398749
035   $a(EXLCZ)995470000002397518
100   $a20090526d2003      ua             0
101 0 $aeng
135   $auran|||||||||
181   $ctxt$2rdacontent
182   $cc$2rdamedia
183   $acr$2rdacarrier
200 00$aGuidance for industry$b[electronic resource] $eproviding regulatory submissions in electronic format, general considerations
210  1$aRockville, MD :$cU.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Biologics Evaluation and Research :$cCenter for Drug Evaluation and Research :$cCenter for Devices and Radiological Health :$cCenter for Food Safety and Applied Nutrition :$cCenter for Veterinary Medicine,$d[2003]
215   $a20 pages $cdigital, PDF file
300   $aTitle from PDF title page (viewed on May 26, 2009).
300   $a"Draft guidance".
300   $a"October 2003".
300   $a"Electronic submissions".
300   $a"Revision 1".
517   $aGuidance for industry 
606   $aElectronic filing systems$xGovernment policy$zUnited States
615  0$aElectronic filing systems$xGovernment policy
712 02$aCenter for Biologics Evaluation and Research (U.S.)
712 02$aCenter for Drug Evaluation and Research (U.S.)
712 02$aCenter for Devices and Radiological Health (U.S.)
712 02$aCenter for Food Safety and Applied Nutrition (U.S.)
712 02$aCenter for Veterinary Medicine (U.S.)
801  0$bGPO
801  1$bGPO
801  2$bGPO
906   $aBOOK
912   $a9910698834903321
996   $aGuidance for industry$93434577
997   $aUNINA