| Record ID | marc_laurentian/openlibrary.mrc:234335820:1334 |
| Source | The Laurentian Library |
| Download Link | /show-records/marc_laurentian/openlibrary.mrc:234335820:1334?format=raw |
LEADER: 01334cam 2200349 a 4500
001 01-0277730
003 CaOEAGC
005 20000215150750.0
008 980106s1996 oncak f000 0 eng d
020 $a0662252926
035 $a(Sirsi) a242391
035 $a(Sirsi) i0662252926
035 $a56911926
040 $dUtOrBLW
043 $an-cn---
050 $aKF'3890.1'S87'1996
245 00 $aStructure and content of clinical study reports :$bICH harmonised tripartite guideline.
260 $aOttawa, Ont. :$bDrugs Directorate,$c1996.
300 $axii, 45 p.
490 1 $aDrugs Directorate guidelines
500 $a"International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use".
500 $aIssued also in French under title: Structure et contenu des rapports d'étude clinique.
596 $a1
650 0 $aDrugs$xResearch$xStandards.
650 0 $aHuman experimentation in medicine$xStandards.
710 2 $aCanada.$bDrugs Directorate.
710 2 $aInternational Conference on Harmonisation.
830 0 $aDrugs Directorate guidelines.
949 $aKF 3890.1 S87 1996$wLC$i30007000670587$rY$tBOOKS$lDESM-CIR$mDESMARAIS
659 $a9900
659 $ae0002
999 $aKF 3890.1 S87 1996$wLC$c1$i30007000670587$lDESM-CIR$mDESMARAIS$rY$sY$tBOOKS$u12/6/2003