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" That the research presents no more than minimal risk of harm to subjects and involves no procedures for which written consent is normally required outside of the research context. "
The Use of Human Biological Materials in the Development of Biomedical ... - Side 174
av United States. Congress. House. Committee on Science and Technology. Subcommittee on Investigations and Oversight - 1986 - 278 sider
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Code of Federal Regulations: Containing a Codification of Documents of ...

1998 - 902 sider
...documentation linking the subject with the research, and the sub-ject's wishes will govern; or (2) That the research presents no more than minimal risk of harm...re-quired outside of the research context. In cases in which the documentation requirement is waived, the IRB may require the investigator to provide subjects...
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Code of Federal Regulations: Education: 34: Parts 1 to 299, Revised as of ...

United States. Office of the Federal Register - 2005 - 648 sider
...documentation linking the subject with the research, and the subject's wishes will govern; or (2) That the research presents no more than minimal risk of harm...required outside of the research context. In cases in which the documentation requirement is waived, the IRB may require the investigator to provide subjects...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1997 - 788 sider
...documentation linking the subject with the research, and the subject's wishes will govern; or (2) That the research presents no more than minimal risk of harm...required outside of the research context. In cases in which the documentation requirement is waived, the IRB may require the investigator to provide subjects...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1995 - 612 sider
...with the research, and the subject's wishes will govern; or (2) That the research presents no m°re than minimal risk of harm to subjects and involves...required outside of the research context. In cases in which the documentation requirement is waived, the IRB may require the investigator to provide subjects...
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The Code of Federal Regulations of the United States of America

1990 - 460 sider
...or the subject's legally authorized representative sign a written consent form if it finds that the research presents no more than minimal risk of harm...which written consent is normally required outside the research context. In cases where the documentation requirement is waived, the IRB may require the...
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The Code of Federal Regulations of the United States of America

1992 - 434 sider
...or the subject's legally authorized representative sign a written consent form if it finds that the research presents no more than minimal risk of harm to subjects and involves no procedures for which 21 CFR Ch. I (4-1-92 Edition) written consent is normally required outside the research context. In...
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The Code of Federal Regulations of the United States of America

2002 - 774 sider
...documentation linking the subject with the research, and the subject's wishes will govern; or (2) That the research presents no more than minimal risk of harm to subjects and involves no procedures for §11.117 Office of the Secretary of Transportation which written consent is normally required outside...
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The Code of Federal Regulations of the United States of America

2002 - 996 sider
...documentation linking the subject with the research, and the subject's wishes will govern; or (2) That the research presents no more than minimal risk of harm to subjects and involves no procedures for §745.118 which written consent is normally required outside of the research context. In cases in which...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1997 - 468 sider
...consent form if it finds that the research presents no more than minimal risk of §56.108 §56.111 harm to subjects and involves no procedures for which written consent is normally required outside the research context; or (2) The I RB may, for some or all subjects, find that the requirements in...
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Code of Federal Regulations: Containing a Codification of Documents of ...

2002 - 780 sider
...documentation linking the subject with the research, and the subject's wishes will govern; or (2) That the research presents no more than minimal risk of harm to subjects and involves no procedures foi which written consent is normally required outside of the research context. In cases in which the...
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