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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 ... - Page 106
1985
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The Code of Federal Regulations of the United States of America

1991 - 712 pages
...this policy, no investigator may involve a human being as a subject in research covered by this policy unless the investigator has obtained the legally effective...description of the procedures to be followed, and identifica49 CFR Subtitle A (10-1-91 Edition) tion of any procedures which are experimental; (2) A...
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The Code of Federal Regulations of the United States of America

2000 - 562 pages
...section, in seeking informed consent the following information shall be provided to each subject: (1) A statement that the study involves research, an explanation...which may reasonably be expected from the research; §27.114 §27.116 (4) A disclosure of appropriate alternative procedures or courses of treatment, if...
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The Code of Federal Regulations of the United States of America

1999 - 650 pages
...section, in seeking informed consent the following information shall be provided to each subject: (1) A statement that the study involves research, an explanation...which may reasonably be expected from the research; Notional Science Foundation (4) A disclosure of appropriate alternative procedures or courses of treatment,...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1995 - 886 pages
...section, in seeking informed consent the following information shall be provided to each subject: (1) A statement that the study involves research, an explanation...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 ...

1998 - 688 pages
...section, in seeking informed consent the following information shall be provided to each subject: (1) A statement that the study involves research, an explanation...identification of any procedures which are experimental; (2) Л description of any reasonably foreseeable risks or discomforts to the subject; (3) A description...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1994 - 708 pages
...section, in seeking informed consent the following information shall be provided to each subject: (1) A statement that the study involves research, an explanation...Identification of any procedures which are experimental; §11.116 (2) A description of any reasonably 'oreseeable risks or discomforts to the tubject; (3) A...
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The Code of Federal Regulations of the United States of America

1990 - 460 pages
...consent. In seeking informed consent, the following information shall be provided to each subject: (1)A statement that the study involves research, an explanation...the subject's participation, a description of the proce§50.20 Food and Drug Administration, HHS dures to be followed, and identification of any procedures...
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The Code of Federal Regulations of the United States of America

1992 - 464 pages
...section, in seeking informed consent the following information shall be provided to each subject: (1)A statement that the study involves research, an explanation...research and the expected duration of the subject's par§1230.116 ticipation, a description of the procedures to be followed, and identification of any...
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Protecting Human Subjects: First Biennial Report on the Adequacy and ...

United States. President's Commission for the Study of Ethical Problems in Medicine and Biomedical and Behavioral Research - 1981 - 286 pages
...elements must be disclosed to subjects for valid informed consent: (a) an explanation of the purpose of the research and the expected duration of the subject's...identification of any procedures which are experimental; (b) a description of any reasonably foreseeable risks or discomforts to the subject; (c) a description...
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Designer Drugs: Hearing Before the Subcommittee on Crime of the Committee on ...

United States. Congress. House. Committee on the Judiciary. Subcommittee on Crime - 1986 - 216 pages
...;\ -: 9 seeking informed consent the following information shall be provided to each subject: (1) A statement that the study involves research, an explanation...subject's participation, a description of the procedures (o be followed, and identification of any procedures which are experimental; (2) A description of any...
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