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200 00$aGuidance for industry$b[electronic resource] $esource animal, product, preclinical, and clinical issues concerning the use of xenotransplantation products in humans
210  1$aRockville, MD :$cU.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Biologics Evaluation and Research,$d[2003]
215   $aii, 60 pages $cdigital, PDF file
300   $aTitle from PDF title page (viewed on May 27, 2009).
300   $a"Final guidance".
300   $a"April 2003".
320   $aIncludes bibliographical references (pages 56-60).
517   $aGuidance for industry 
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300   $a"July 25, 2002."
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