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" IRB shall determine that all of the following requirements are satisfied: (1) Risks to subjects are minimized: (i) By using procedures which are consistent with sound research design and which do not unnecessarily expose subjects to risk, and (ii) whenever... "
The Code of Federal Regulations of the United States of America - Side 130
1992
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Code of Federal Regulations: Containing a Codification of Documents of ...

1998 - 902 sider
...research design and which do not unnecessarily expose subjects to risk, and (11) Whenever appropriate, by using procedures already being performed on the...from the research (as distin-guished from risks and benefits of therapies subjects would receive even If not participating in the research). The IRB should...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1995 - 606 sider
...research design and which do not unnecessarily expose subjects to risk, and (ii) whenever appropriate, by using procedures already being performed on the...from the research (as distinguished from risks and benefits of therapies subjects would receive even if not participating in the research). The IRB should...
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The Code of Federal Regulations of the United States of America

2006 - 626 sider
...research design and which do not unnecessarily expose subjects to risk, and (ii) whenever appropriate, by using procedures already being performed on the...risks and benefits that may result from the research fas distinguished from risks and benefits of therapies subjects would receive even if not participating...
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The Code of Federal Regulations of the United States of America

2002 - 802 sider
...research design and which do not unnecessarily expose subjects to risk, and (ii) whenever appropriate, by using procedures already being performed on the...should consider only those risks and benefits that may 38 CFR Ch. I (7-1-02 Edition result from the research (as distinguished from risks and benefits of...
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The Code of Federal Regulations of the United States of America

2003 - 496 sider
...research design and which do not unnecessarily expose subjects to risk, and (ii) whenever appropriate, by using procedures already being performed on the...should consider only those risks and benefits that may 279 200-046 D-10 result from the research (as distinguished from risks and benefits of therapies subjects...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1998 - 760 sider
...research design and which do not unnecessarily expose subjects to risk, and (11) whenever appropriate, by using procedures already being performed on the...expected to result. In evaluating risks and benefits, the ГОВ should consider only those risks and benefits that may result from the research (as distinguished...
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The Code of Federal Regulations of the United States of America

2004 - 556 sider
...research design and which do not unnecessarily expose subjects to risk, and (ii) whenever appropriate, by using procedures already being performed on the...the importance of the knowledge that may reasonably & expected to result. In evaluating risto and benefits, the IRB should consider only those risks and...
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The Code of Federal Regulations of the United States of America

1990 - 460 sider
...research design and which do not unnecessarily expose subjects to risk, and (ii) whenever appropriate, by using procedures already being performed on the...subjects, and the importance of the knowledge that may be expected to result. In evaluating risks and benefits, the IRB should consider only those risks and...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1998 - 902 sider
...ezpoee subjects to risk, and (il) Whenever appropriate, by using procedures already being performed or the subjects for diagnostic or treatment purposes....may reasonably be expected to result. In evaluating riete and benefits, the IRB should consider only those risks and benefits that may result from the...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1995 - 886 sider
...subjects are reasonable in relation to anticipated benefits, ii any, to subjects, and the importance ol the knowledge that may reasonably be expected to result....from the research (as distinguished from risks and benefits of therapies subjects would receive even il not participating in the research). The IRB should...
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