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 1
... scientific study that is the basis for determining what drugs ought to be controlled and in what schedule they can most approximately be controlled . Since the law became effective , as part of the Comprehensive Crime Control Act of ...
... scientific study that is the basis for determining what drugs ought to be controlled and in what schedule they can most approximately be controlled . Since the law became effective , as part of the Comprehensive Crime Control Act of ...
Side 32
... scientific experi- mentation is capable of producing . The S. 1437 would provide the legislation needed to combat the problem of controlled substance analogs by adding a new sec- tion 403A to the Controlled Substances Act to create ...
... scientific experi- mentation is capable of producing . The S. 1437 would provide the legislation needed to combat the problem of controlled substance analogs by adding a new sec- tion 403A to the Controlled Substances Act to create ...
Side 34
... scientific research while effectively proscribing activity involving danger- ous controlled substance analogs ; ( 2 ) departing from the basic approach of the Controlled Substances Act that relies on the scheduling of substances before ...
... scientific research while effectively proscribing activity involving danger- ous controlled substance analogs ; ( 2 ) departing from the basic approach of the Controlled Substances Act that relies on the scheduling of substances before ...
Side 38
... scientific research . Thus , the problems described earlier regarding the application of the new - drug approval process had to be solved in order to provide a realistic exemption through operation of the Federal Food , Drug , and ...
... scientific research . Thus , the problems described earlier regarding the application of the new - drug approval process had to be solved in order to provide a realistic exemption through operation of the Federal Food , Drug , and ...
Side 45
... the PHS was the early identification of MPTP and the development of the animal model for Parkinson's disease . These scientific findings not only illuminated the dangers of clandestinely produced drugs , they also provided researchers 45.
... the PHS was the early identification of MPTP and the development of the animal model for Parkinson's disease . These scientific findings not only illuminated the dangers of clandestinely produced drugs , they also provided researchers 45.
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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
Populære avsnitt
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...