Designer Drugs: Hearing Before the Subcommittee on Crime of the Committee on the Judiciary, House of Representatives, Ninety-ninth Congress, First Session, on H.R. 2014, H.R. 2977, H.R. 3936, and S. 1437, May 1, 1986U.S. Government Printing Office, 1986 - 199 sider |
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Side 60
... the Nuremberg Code , among a number , is that studies in experimental animals need to be done before substances are given to humans for the first time . Informed consent is another one . But in terms of our requirements for animal 60.
... the Nuremberg Code , among a number , is that studies in experimental animals need to be done before substances are given to humans for the first time . Informed consent is another one . But in terms of our requirements for animal 60.
Side 61
... of the Nuremberg Code , among a number , is that studies in experimental animals need to be done before substances are given to humans for the first time Informed consent is another one . But in terms of our requirements for animal 60.
... of the Nuremberg Code , among a number , is that studies in experimental animals need to be done before substances are given to humans for the first time Informed consent is another one . But in terms of our requirements for animal 60.
Side 176
... consent . 46.117 Documentation of informed consent . 46.118 Applications and proposals lacking definite plans for involvement of human subjects . 46.119 Research undertaken without the intention of involving human subjects . 46.120 ...
... consent . 46.117 Documentation of informed consent . 46.118 Applications and proposals lacking definite plans for involvement of human subjects . 46.119 Research undertaken without the intention of involving human subjects . 46.120 ...
Side 177
... consent of each participant or subject . § 46.102 Definitions . ( a ) ' ' Secretary ' ' means the Secretary of Health and Human Services and any other officer or employee of the Department of Health and Human Services to whom authority ...
... consent of each participant or subject . § 46.102 Definitions . ( a ) ' ' Secretary ' ' means the Secretary of Health and Human Services and any other officer or employee of the Department of Health and Human Services to whom authority ...
Side 179
... consent is in accordance with § 46.116 . The IRB may require that information , in addition to that specifically mentioned in § 46.116 , be given to the subjects when in the IRB's judgment the information would meaningfully add to the ...
... consent is in accordance with § 46.116 . The IRB may require that information , in addition to that specifically mentioned in § 46.116 , be given to the subjects when in the IRB's judgment the information would meaningfully add to the ...
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Administration amended amphetamine appropriate approved Attorney bill California Chairman chemical structure chemist clandestine laboratory Committee compounds conducted Congress controlled substance analogs Controlled Substances Act Cosmetic Act criminal Department of Health designer drug manufacture designer drug problem drug abuse Drug Enforcement Administration effect ELLINWOOD emergency scheduling exemption Federal Food fentanyl analogs fetus Florida Food and Drug going GRINSPOON HAWKS Health and Human heroin HUGHES human consumption Human Services human subjects identified illegal individual informed consent Institutional Review Board intended for human intent to distribute investigator law enforcement legislation legitimate research LUNGREN MCCOLLUM MDMA meperidine MPPP MPTP narcotic analogs NIDA paragraph Parkinson's disease potential produce programs psychoactive drugs public health regulations research activities research involving Senator CHILES specific statement statute street studies subpart substance in Schedules substantially similar Thank therapeutic tion Tocus toxicity trolled substance violation
Populære avsnitt
Side 120 - Risks to subjects are reasonable in relation to anticipated benefits, if any, to subjects, and the importance of the knowledge that may reasonably be expected to result.
Side 122 - ... risks to the subject (or to the embryo or fetus, if the subject is or may become pregnant) which are currently unforeseeable; 2. anticipated circumstances under which the subject's participation may be terminated by the investigator without regard to the subject's consent; 3.
Side 119 - Each IRB shall have at least five members, with varying backgrounds to promote complete and adequate review of research activities commonly conducted by the institution. The IRB shall be sufficiently qualified through the experience and expertise of its members, and the diversity of the members...
Side 119 - IRB shall require documentation of informed consent or may waive documentation in accordance with §46.117. (d) An IRB shall notify investigators and the institution in writing of its decision to approve or disapprove the proposed research activity, or of modifications required to secure IRB approval of the research activity.
Side 25 - I would be pleased to respond to any questions you or members of the committee may have.
Side 128 - Requirements for permission by parents or guardians and for assent by children. (a) In addition to the determinations required under other applicable sections of this subpart. the IRB shall determine that adequate provisions are made for soliciting the assent of the children, when in the judgment of the IRB the children are capable of providing assent.
Side 121 - ... reports submitted by investigators, and reports of injuries to subjects. (2) Minutes of IRB meetings which shall be in sufficient detail to show attendance at the meetings; actions taken by the IRB; the vote on these actions including the number of members voting for, against, and abstaining; the basis for requiring changes in or disapproving research; and a written summary of the discussion of controverted issues and their resolution. (3) Records of continuing review activities. (4) Copies of...
Side 128 - Research not otherwise approvable which presents an opportunity to understand, prevent, or alleviate a serious problem affecting the health or welfare of children...
Side 119 - Except when an expedited review procedure is used (see § 46. 1 10), review proposed research at convened meetings at which a majority of the members of the IRB are present, including at least one member whose primary concerns are in nonscientific areas. In order for the research to be approved, it shall receive the approval of a majority of those members present at the meeting.