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001 9910698132503321
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035   $a(CKB)5470000002395658
035   $a(OCoLC)316802213
035   $a(EXLCZ)995470000002395658
100   $a20090323d2009      ua             0
101 0 $aeng
135   $aurbn|||||||||
181   $ctxt$2rdacontent
182   $cc$2rdamedia
183   $acr$2rdacarrier
200 00$aGuidance for industry$b[electronic resource] $eCurrent Good Tissue Practice (CGTP) and additional requirements for manufacturers of human cells, tissues, and cellular and tissue based products (HCT/Ps)
210  1$aRockville, MD :$cU.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Biologics Evaluation and Research,$d[2009]
215   $ai, 59 pages $cdigital, PDF file
300   $aTitle from PDF title page (viewed on Mar. 23, 2009).
300   $a"Draft guidance."
300   $a"January 2009."
320   $aIncludes bibliographical references (pages 58-59).
517   $aGuidance for industry 
606   $aTissue culture
615  0$aTissue culture.
712 02$aCenter for Biologics Evaluation and Research (U.S.)
801  0$bGPO
801  1$bGPO
801  2$bGPO
906   $aBOOK
912   $a9910698132503321
996   $aGuidance for industry$93434577
997   $aUNINA