(Q56784198)

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Determination of required content of the informed consent process for human participants in biomedical research conducted in the U.S. A practical tool to assist clinical investigators

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Determination of required content of the informed consent process for human participants in biomedical research conducted in the U.S. A practical tool to assist clinical investigators (English)

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Cheryl M Chanaud

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language of work or name

English

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publication date

July 2008

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published in

Contemporary Clinical Trials

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volume

29

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issue

4

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page(s)

501-6

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DOI

10.1016/J.CCT.2007.11.006

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PubMed publication ID

18249042

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(Q56784198)

Determination of required content of the informed consent process for human participants in biomedical research conducted in the U.S. A practical tool to assist clinical investigators

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