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100   $a20090814d2007      ua             0
101 0 $aeng
135   $auran|||||||||
181   $ctxt$2rdacontent
182   $cc$2rdamedia
183   $acr$2rdacarrier
200 00$aGuidance for industry$b[electronic resource] $eprotecting the rights, safety and welfare of study subjects : supervisory responsibilities of investigators
210  1$aRockville, MD :$cU.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research :$cCenter for Biologics Evaluation and Research :$cCenter for Devices and Radiological Health,$d[2007]
215   $a1 online resource (unpaged) $cforms
300   $a"Draft guidance".
300   $a"May 2007".
517   $aGuidance for industry 
606   $aHuman experimentation in medicine$xGovernment policy$zUnited States
606   $aMedical research personnel$xGovernment policy$zUnited States
615  0$aHuman experimentation in medicine$xGovernment policy
615  0$aMedical research personnel$xGovernment policy
712 02$aCenter for Drug Evaluation and Research (U.S.)
712 02$aCenter for Biologics Evaluation and Research (U.S.)
712 02$aCenter for Devices and Radiological Health (U.S.)
801  0$bGPO
801  1$bGPO
906   $aBOOK
912   $a9910699066103321
996   $aGuidance for industry$93434577
997   $aUNINA