| Do informed consent documents matter? | |
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MedLine Citation:
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PMID: 18977313 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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This commentary argues that, despite extensive critiques of informed consent documents, there are several ethical and legal reasons for investigators and IRB members to take these documents seriously. |
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Authors:
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David B Resnik |
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Publication Detail:
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Type: Journal Article; Research Support, N.I.H., Intramural Date: 2008-11-01 |
Journal Detail:
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Title: Contemporary clinical trials Volume: 30 ISSN: 1559-2030 ISO Abbreviation: Contemp Clin Trials Publication Date: 2009 Mar |
Date Detail:
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Created Date: 2009-02-23 Completed Date: 2010-01-15 Revised Date: 2012-03-07 |
Medline Journal Info:
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Nlm Unique ID: 101242342 Medline TA: Contemp Clin Trials Country: United States |
Other Details:
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Languages: eng Pagination: 114-5 Citation Subset: IM |
Affiliation:
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NIEHS/NIH, Research Triangle Park, NC 27709, United States. resnikd@niehs.nih.gov |
Export Citation:
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APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
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Documentation
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standards Ethics Committees, Research / ethics*, legislation & jurisprudence, standards Ethics, Research* Humans Informed Consent / ethics*, legislation & jurisprudence, standards United States |
| Grant Support | |
ID/Acronym/Agency:
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Z99 ES999999/ES/NIEHS NIH HHS |
| Comments/Corrections | |
Comment In:
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Contemp Clin Trials. 2009 Sep;30(5):388-9
[PMID:
19539782
]
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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