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" An IRB may waive the requirement for the investigator to obtain a signed consent form for some or all subjects if it finds either: (1) That the only record linking the subject and the research would be the consent document and the principal risk would... "
AIDS Issues: Hearings Before the Subcommittee on Health and the Environment ... - Page 166
by United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health and the Environment - 1985 - 357 pages
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The Code of Federal Regulations of the United States of America

2005 - 718 pages
...given to the subject or the representative, in addition to a copy of the short form. (c) An IRB may waive the requirement for the investigator to obtain...consent form for some or all subjects if it finds either: (1) That the only record linking the subject and the research would be the consent document...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1998 - 902 pages
...given to the subject or the representative, in addition to a copy of the short form. (c) An IRB may waive the require-ment for the investigator to obtain...consent form for some or all subjects if it finds either: (1) That the only record linking the subject and the research would be the consent document...
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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
...to the subject or the representative, in addition to a copy of the "short form . ' ' (c) An IRB may waive the requirement for the investigator to obtain...consent form for some or all subjects if it finds either: (1) That the only record linking the subject and the research would be the consent document...
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The Code of Federal Regulations of the United States of America

1998 - 668 pages
...given to the subject or the representative, in addition to a copy of the short form. (c) An IRB may waive the requirement for the investigator to obtain...consent form for some or all subjects if it finds either: (1) That the only record linking the subject and the research would be the consent document...
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Biomedical-ethical Issues: A Digest of Law and Policy Development

Frank Harron - 1983 - 192 pages
...given to the subject or the representative, in addition to a copy of the "short form." (c) An IRB may waive the requirement for the investigator to obtain a signed consent form of some or all subjects if it finds either: (1) That the only record linking the subject and the research...
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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 - 312 pages
...given to the subject or the representative, in addition to a copy of the "short form. " (c) An IRB may waive the requirement for the investigator to obtain...consent form for some or all subjects if it finds either: (1) That the only record linking the subject and the research would be the consent document...
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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 - 304 pages
...be given to the subject or the representative, in addition to a copy of the ' 'short (c)* An IRB may waive the requirement for the investigator to obtain...consent form for some or all subjects if it finds either ( 1) That the only record linking the subject and the research would be the consent document...
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Ethics and Regulation of Clinical Research

Robert J. Levine - 1988 - 484 pages
...given to the subject or the representative, in addition to a copy of the "short form." (c) An IRB may waive the requirement for the investigator to obtain...consent form for some or all subjects if it finds either: (1) That the only record linking the subject and the research would be the consent document...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1991 - 738 pages
...the representative, in addition to a copy of foe short form. (c) An IRB may waive the require"«it for the investigator to obtain a signed consent form for some or all Ejects if ft fmds either: (1) That the only record linking the subject and the research would be the...
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Children As Research Subjects : Science, Ethics, and Law: Science, Ethics ...

Program in Medical Ethics Michael A. Grodin Director, Leonard H. Glantz Associate Director and Professor of Health Law both at the Boston University Schools of Medicine and Public Health - 1994 - 290 pages
...given to the subject or the representative, in addition to a copy of the short form. (c) An IRB may waive the requirement for the investigator to obtain...consent form for some or all subjects if it finds either: (1) that the only record linking the subject and the research would be the consent document...
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