LEADER 01811oam 2200541 450 001 9910711779603321 005 20220408143846.0 035 $a(CKB)5470000002486273 035 $a(OCoLC)1080339765 035 $a(EXLCZ)995470000002486273 100 $a20181228d2018 ua 0 101 0 $aeng 135 $aurbn||||a|||| 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 10$aExamining patient access to investigational drugs $ehearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Fifteenth Congress, first session. October 3, 2017 210 1$aWashington :$cU.S. Government Publishing Office,$d2018. 215 $a1 online resource (iv, 235 pages) $cphotographs 300 $a"Serial No. 115-60." 320 $aIncludes bibliographical references. 517 $aExamining patient access to investigational drugs 606 $aClinical trials$zUnited States 606 $aClinical trials$xMoral and ethical aspects$zUnited States 606 $aDrugs$zUnited States$xTesting 606 $aDrugs$xTesting$xMoral and ethical aspects$zUnited States 608 $aLegislative hearings.$2lcgft 615 0$aClinical trials 615 0$aClinical trials$xMoral and ethical aspects 615 0$aDrugs$xTesting. 615 0$aDrugs$xTesting$xMoral and ethical aspects 801 0$bGPO 801 1$bGPO 801 2$bGPO 801 2$bMERUC 801 2$bIAD 801 2$bOCLCO 801 2$bUPM 801 2$bOCLCF 801 2$bSOI 801 2$bOCLCO 801 2$bIAS 801 2$bOCLCQ 801 2$bGPO 906 $aBOOK 912 $a9910711779603321 996 $aExamining patient access to investigational drugs$93515940 997 $aUNINA