 | 1996 - 624 páginas
...authorized representative. A copy shall be given to the person signing the form. (b) Except as provided in paragraph (c) of this section, the consent form...of harm to subjects and involves no procedures for which written consent is normally required outside of the research context. In cases in which the documentation... | |
 | 2006 - 626 páginas
...authorized representative. A copy shall be given to the person signing the form. (b) Except as provided in paragraph (c) of this section, the consent form...harm resulting from a breach of confidentiality. Each §lc.H7 Office of the Secretary, USDA subject will be asked whether the subject wants documentation... | |
 | 2000 - 680 páginas
...short form written consent document stating that the elements of informed consent required by §46.116 have been presented orally to the subject or the subject's...of harm to subjects and involves no procedures for which written consent is normally required outside of the research context. In cases in which the documentation... | |
 | 2000 - 928 páginas
...short form written consent document stating that the elements of informed consent required by §745.116 have been presented orally to the subject or the subject's...of harm to subjects and involves no procedures for which written consent is normally required outside of the research context. In cases in which the documentation... | |
 | 1988 - 584 páginas
...form" written consent document stating that the elements of Informed consent required by § 46.116 hare been presented orally to the subject or the subject's...of harm to subjects and involves no procedures for which written consent is normally required outside of the research context. In cases where the documentation... | |
 | 1995 - 1136 páginas
...orally to the subject or the subject's legally authorized representative. When this method is tued, there shall be a witness to the oral presentation....of harm to subjects and Involves no procedures for which written consent is normally required outside of the research context. In cases in which the documentation... | |
 | 1985 - 474 páginas
...subject's legally authorized presentative. When this method is «d, there shall be a witness to the al presentation. Also, the IRB shall approve a written...of harm to subjects and involves no procedures for which written consent is normally required outside of the research context. In cases where the documentation... | |
 | 1993 - 650 páginas
...representative. When this method is used, there shall be a witness to the oral presentation. Also, the IBB shall approve a written summary of what is to be said...of harm to subjects and involves no procedures for which written consent is normally required outside of the research context. In cases in which the documentation... | |
 | 1999 - 670 páginas
...representative. When this method is used, there shall be a witness to the oral presentation. Also, the IBB shall approve a written summary of what is to be said...of harm to subjects and involves no procedures for which written consent is normally required outside of the research context. In cases in which the documentation... | |
 | 1998 - 902 páginas
...representative. When this method is used, there shall be a witness to the oral presentation. Also, the ГОВ shall approve a written summary of what is to be said...of harm to subjects and Involves no procedures for which written consent is normally re-quired outside of the research context. In cases in which the... | |
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... short form. (c) 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... 
