 | 1998 - 902 sider
...elements of Informed consent. Except as provided in paragraph (c) or (d) of this section, in seeking informed consent the following information shall be...otherwise entitled, and the subject may discontinue parló CFR Ch. It (1-1-98 Edffion) ticlpation at any time without penalty or loss of benefits to which... | |
 | 1995 - 754 sider
...elements of informed consent. Except as provided in paragraph (c) or (d) of this section, in seeking informed consent the following information shall be...benefits to which the subject is otherwise entitled. 294 and the subject may discontinue participation at any time without penalty or loss of benefits to... | |
 | 2004 - 556 sider
...elements of informed consent. Except as provided in paragraph (c) or (d) of this section, in seeking informed consent the following information shall be...participation is voluntary, refusal to participate wfil involve no penalty or loss of benefits to which the subject is otherwise entitled, and the subject... | |
 | 2004 - 1132 sider
...extent, if any, to which confidentiality of records identifying the subject will be maintained; (61 For research involving more than minimal risk, an...event of a research-related injury to the subject; and 407 203-121 0-14 (8) A statement that participation is voluntary, refusal to participate will involve... | |
 | 1990 - 460 sider
...maintained and that notes the possibility that the Food and Drug Administration may inspect the records. (6) For research involving more than minimal risk,...event of a research-related injury to the subject. (8) A statement that participation is voluntary, that refusal to participate will involve no penalty... | |
 | 1995 - 440 sider
...than minimal risk, an explanation as to whether any compensation and an ex§50.25 §50.40 planatlon as to whether any medical treatments are available...event of a research-related injury to the subject. (8) A statement that participation is voluntary, that refusal to participate will involve no penalty... | |
 | Frank Harron - 1983 - 192 sider
...Basic elements of informed consent. Except as provided in paragraph (c) of this section, in seeking informed consent the following information shall be...event of a research-related injury to the subject; and 132 Informed Consent (8) A statement that participation is voluntary, refusal to participate will involve... | |
 | 1987 - 440 sider
...maintained and that notes the possibility that the Food and Drug Administration may inspect the records. (6) For research involving more than minimal risk,...event of a research-related injury to the subject. (8) A statement that participation is voluntary, that refusal to participate will involve no penalty... | |
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A disclosure of appropriate alternative procedures or courses of treatment, if any, that might be advantageous to the subject; (5) A statement describing the extent, if any, to which confidentiality of records identifying the subject will be maintained;... 
