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" A statement that the study involves research, an explanation of the purposes of the research and the expected duration of the subject's participation, a description of the procedures to be followed, and identification of any procedures which are experimental... "
Code of Federal Regulations: Containing a Codification of Documents of ... - Side 129
1997
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The Code of Federal Regulations of the United States of America

1994 - 612 sider
...reasonable manner. (Approved by the Office of Management and Budget under control number 9999-0020) §46.116 General requirements for informed consent. Except...which may reasonably be expected from the research; §46.114 Department of Health and Human Services (4) A disclosure of appropriate alternative procedures...
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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
...USC 300v-l(b)) [56 FR 28012, 28021, June 18, 1991, as amended at 70 FR 36328, June 23, 2005] §97.116 General requirements for informed consent. Except...which may reasonably be expected from the research; §97.116 (4) A disclosure of appropriate alternative procedures or courses of treatment, if any, that...
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The Code of Federal Regulations of the United States of America

1997 - 652 sider
...reasonable manner. (Approved by the Office of Management and Budget under control number 9999-0020) §46.116 General requirements for informed consent. Except...reasonably foreseeable risks or discomforts to the subject; §46.114 Department of Health and Human Services (3) A description of any benefits to the subject or...
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The Code of Federal Regulations of the United States of America

1998 - 956 sider
...by the Office of Management and Budget under control number 9999-0020) 9745.116 General requirement* for informed consent. Except as provided elsewhere...reasonably foreseeable risks or discomforts to the subject; §745.116 (3) A description of any benefits to the subject or to others which may reasonably be expected...
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The Code of Federal Regulations of the United States of America

1998 - 668 sider
...of Management and Budget under control number 9999-0020) §46.116 General requirements for in formed consent. Except as provided elsewhere in this policy,...reasonably foreseeable risks or discomforts to the subject; §46.114 Deportment of Health and Human Services (3) A description of any benefits to the subject or...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1995 - 886 sider
...by the Office of Management and Budget under control number 9999-0020) 516.116 General requirement« for informed consent. Except as provided elsewhere...identification of any procedures which are experimental; (2) A | foresees subject! (3) A the sub] sonablj (4) A native ment, tageous (5) Al tent, if I recordsl maintaj...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1999 - 670 sider
...manner. (Approved by the Office of Management and Budget under control number 9999-0020) §690.116 General requirements for informed consent. Except...followed, and identification of any procedures which are experi mental; (2) A description of any reasonably foreseeable risks or discomforts to the subject;...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1998 - 956 sider
...the institution or its agents from liability for negligence. (a) Basic elements of informed corami. Except as provided In paragraph (c) or (d) of this...reasonably foreseeable risks or discomforts to the subject; §745.114 Deportment of Energy (3) A description of any benefits to the subject or to others which...
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The Code of Federal Regulations of the United States of America

1994 - 1184 sider
...provided to each subject: (1) A statement that the study involves research, an explanation of the §26.116 purposes of the research and the expected duration...foreseeable risks or discomforts to the subject; (3) Л description of any benefits to the subject or to others which may reasonably be expected from the...
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The Use of Human Biological Materials in the Development of Biomedical ...

United States. Congress. House. Committee on Science and Technology. Subcommittee on Investigations and Oversight - 1986 - 304 sider
...RESEARCH/ AN EXPLANATION OF THE PURPOSES OF THE RESEARCH AND THE EXPECTED DURATION OF THE SUBJECTS' PARTICIPATION/ A DESCRIPTION OF THE PROCEDURES TO...REASONABLY FORESEEABLE RISKS OR DISCOMFORTS TO THE SUBJECT; PAGE 6 3- A DESCRIPTION OF ANY BENEFITS TO THE SUBJECT OR TO OTHERS WHICH MAY REASONABLY BE EXPECTED...
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