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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... Department of Health and Human Services , accompanied by Vernon Houk , M.D. , Director , Center for Environmental Health , Centers for Dis- ease Control , U.S. Department of Health and Human Services ; Edward C. Tocus , Ph.D. , Director ...
... Department of Health and Human Services , accompanied by Vernon Houk , M.D. , Director , Center for Environmental Health , Centers for Dis- ease Control , U.S. Department of Health and Human Services ; Edward C. Tocus , Ph.D. , Director ...
Side 8
... Department of Justice authorization bill . The law should not be a game to those who would abuse it . We must work together to close these loopholes which have allowed the designers of deadly substances to play this game thus far . Mr ...
... Department of Justice authorization bill . The law should not be a game to those who would abuse it . We must work together to close these loopholes which have allowed the designers of deadly substances to play this game thus far . Mr ...
Side 10
... Department of Alcohol and Drug Programs . I think it is an instructive film . It is only about 6 min- utes , and it goes into the question that we are talking about . [ Video tape presentation : " The Walking Death . " ] Mr. HUGHES . I ...
... Department of Alcohol and Drug Programs . I think it is an instructive film . It is only about 6 min- utes , and it goes into the question that we are talking about . [ Video tape presentation : " The Walking Death . " ] Mr. HUGHES . I ...
Side 25
... Department , as I know you were , to come up with proper legislation , it was very difficult to figure how we would define the universe we were talking about . Senator CHILES . Yes , sir . Mr. LUNGREN . And initially , some people said ...
... Department , as I know you were , to come up with proper legislation , it was very difficult to figure how we would define the universe we were talking about . Senator CHILES . Yes , sir . Mr. LUNGREN . And initially , some people said ...
Side 25
... Department , as I know you were , to come up with proper legislation , it was very difficult to figure how we would define the universe we were talking about . Senator CHILES . Yes , sir . Mr. LUNGREN . And initially , some people said ...
... Department , as I know you were , to come up with proper legislation , it was very difficult to figure how we would define the universe we were talking about . Senator CHILES . Yes , sir . Mr. LUNGREN . And initially , some people said ...
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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.