Record ID | marc_loc_updates/v36.i11.records.utf8:15971850:1602 |
Source | Library of Congress |
Download Link | /show-records/marc_loc_updates/v36.i11.records.utf8:15971850:1602?format=raw |
LEADER: 01602cam a22003254a 4500
001 2007281216
003 DLC
005 20080312154733.0
008 071024s2007 dcuak b 000 0 eng c
010 $a 2007281216
020 $a1422437493
020 $a9781422437490
020 $a1422437485 (members)
020 $a9781422437483 (members)
035 $a(OCoLC)ocm81281955
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 $aviii, 135 p. :$bill., forms ;$c28 cm. +$e1 CD-ROM (4 3/4 in.)
440 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.