| Record ID | harvard_bibliographic_metadata/ab.bib.10.20150123.full.mrc:138895245:1618 |
| Source | harvard_bibliographic_metadata |
| Download Link | /show-records/harvard_bibliographic_metadata/ab.bib.10.20150123.full.mrc:138895245:1618?format=raw |
LEADER: 01618cam a2200337 a 4500
001 010202964-4
005 20090331132652.0
008 071024s2007 dcuk b 001 0 eng c
010 $a 2007281216
020 $a1422437493
020 $a9781422437490
020 $a1422437485 (members)
020 $a9781422437483 (members)
035 0 $aocm81281955
040 $aInIU-L$cILI$dILI$dDLC
042 $apcc
043 $an-us---
050 00 $aR853.H8$bI573 2007
082 00 $a174.2/8$222
245 00 $aInstitutional review boards :$ba primer /$cTeresa A. Williams ... [et al.].
260 $aWashington, DC :$bAmerican Health Lawyers Association,$cc2007.
300 $aviii, 135 p. :$bforms ;$c28 cm. +$e1 CD-ROM (4 3/4 in.)
490 0 $aHealth lawyers, expert series
504 $aIncludes bibliographical references and index.
505 0 $aDistinguishing work from other activities -- Regulations that govern research -- Understanding the clinical trial process -- Institutional review boards -- The IRB process -- Special categories of review -- Understanding research informed consent -- Additional requirements of HIPAA -- Conflict of interest issues -- Relevant case law -- Typical areas of IRB noncompliance and practical advice --Conclusion & additional guidance for the research process -- Exhibits -- Additional exhibits & forms.
650 0 $aInstitutional review boards (Medicine)$zUnited States.
650 0 $aHuman experimentation in medicine$zUnited States$xEvaluation.
700 1 $aWilliams, Teresa A.
710 2 $aAmerican Health Lawyers Association.
988 $a20070108
906 $0OCLC