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 18
... possession with intent to distribute or the distribution . In order to avoid the necessity of listing , thus advertis- ing the specific controlled analog , the legislation would outlaw de- signer rs , any substance other than a ...
... possession with intent to distribute or the distribution . In order to avoid the necessity of listing , thus advertis- ing the specific controlled analog , the legislation would outlaw de- signer rs , any substance other than a ...
Side 33
... or part of which is intended for human consumption without having complied with the provisions of the Federal Food , Drug , and Cosmetic Act . The bill also makes - 5 - simple possession of a controlled substance analog 33.
... or part of which is intended for human consumption without having complied with the provisions of the Federal Food , Drug , and Cosmetic Act . The bill also makes - 5 - simple possession of a controlled substance analog 33.
Side 34
... possession of a controlled substance analog all or part of which is intended for human consumption a crime punishable by imprisonment for a year and a fine of $ 25,000 unless there is compliance with the latter Act . CONSIDERATIONS IN ...
... possession of a controlled substance analog all or part of which is intended for human consumption a crime punishable by imprisonment for a year and a fine of $ 25,000 unless there is compliance with the latter Act . CONSIDERATIONS IN ...
Side 35
... possession , or distribution of a substance in conformance with the new - drug approval provision of the Federal Food , Drug , and Cosmetic Act , and early - stage re- search activity affected by the bill is protected by reference to ...
... possession , or distribution of a substance in conformance with the new - drug approval provision of the Federal Food , Drug , and Cosmetic Act , and early - stage re- search activity affected by the bill is protected by reference to ...
Side 92
... possession of the newly scheduled drug . And , importantly , legitimate scientists in pharmaceutical companies , academia and elsewhere do not have to be concerned that , in conducting research , they are unwittingly violating the law ...
... possession of the newly scheduled drug . And , importantly , legitimate scientists in pharmaceutical companies , academia and elsewhere do not have to be concerned that , in conducting research , they are unwittingly violating the law ...
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amended amphetamine appropriate approval Attorney bill California Chairman chemical structure chemists clandestine laboratories Committee compounds conducted CONGRESS THE LIBRARY controlled substance analogs Controlled Substances Act Cosmetic Act criminal Department of Health designer drug manufacture designer drug problem drug abuse Drug Enforcement Drug Enforcement Administration drug or substance effect emergency scheduling exemption Federal Food fentanyl analogs fetus Florida Food and Drug GRINSPOON HAWKS Health and Human heroin HUGHES human consumption Human Services human subjects illegal illicit drug individuals informed consent Institutional Review Board intended for human intent to distribute investigational law enforcement legislation legitimate research LIBRARY OF CONGRESS LUNGREN MCCOLLUM MDMA meperidine MPPP MPTP NIDA paragraph Parkinson's disease potential procedures produce programs public health regulations research involving Secretary of Health Senator CHILES specific statement studies subpart substance in Schedules substantially similar synthetic Thank therapeutic tion Tocus toxicity trolled substance
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Side 39 - I would be pleased to respond to any questions you or members of the committee may have.
Side 178 - Minimal risk means that the probability and magnitude of harm or discomfort anticipated in the research are not greater in and of themselves than those ordinarily encountered in daily life or during the performance of routine physical or psychological examinations or tests.
Side 178 - Private information includes information about behavior that occurs in a context in which an individual can reasonably expect that no observation or recording is taking place, and information which has been provided for specific purposes by an individual and which the individual can reasonably expect will not be made public (for example, a medical record). Private information must be individually identifiable (ie, the identity of the subject is or may readily be ascertained by the investigator or...
Side 33 - No person shall introduce or deliver for introduction into interstate commerce any new drug, unless an approval of an application filed pursuant to subsection (b) is effective with respect to such drug.
Side 178 - ... for determining which projects require review more often than annually and which projects need verification from sources other than the investigators that no material changes have occurred since previous IRB review...
Side 177 - Research involving the collection or study of existing data, documents, records, pathological specimens, or diagnostic specimens, if these sources are publicly available, or if the information is recorded by the investigator in such a manner that subjects cannot be identified, directly or through identifiers linked to the subjects.
Side 179 - 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.
Side 185 - The purpose of the activity is to meet the health needs of the mother and the fetus will be placed at risk only to the minimum extent necessary to meet such needs, or (2) the risk to the fetus is minimal.
Side 178 - A statement of principles governing the institution in the discharge of its responsibilities for protecting the rights and welfare of human subjects of research conducted at or sponsored by the institution, regardless of whether the research is subject to federal regulation.
Side 188 - The risk represents a minor increase over minimal risk; (b) The intervention or procedure presents experiences to subjects that are reasonably commensurate with those inherent in their actual or expected medical, dental, psychological, social, or educational situations; 45 CFR Subtitle A (10-1-93 Edition) (c) The intervention or procedure is likely to yield generalizable knowledge about the subjects...