Institutional Review Boards, a System in Jeopardy: Hearing Before the Subcommittee on Human Resources of the Committee on Government Reform and Oversight, House of Representatives, One Hundred Fifth Congress, Second Session, June 11, 1998 |
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Page 10
... increase in inter- est in the research subjects wanting to participate in the research , wanting to get drugs that are available , perhaps wanting to make some money to help them through school . And we see new types of research that ...
... increase in inter- est in the research subjects wanting to participate in the research , wanting to get drugs that are available , perhaps wanting to make some money to help them through school . And we see new types of research that ...
Page 12
... increase the Federal investment in cancer and other biomedical research and a number of recent proposals recommending greater responsibilities for IRBs in the areas of genetics and patient confidentiality . My testimony is based on more ...
... increase the Federal investment in cancer and other biomedical research and a number of recent proposals recommending greater responsibilities for IRBs in the areas of genetics and patient confidentiality . My testimony is based on more ...
Page 16
... increasing cost pressures due to the rise of managed care and capitated payments . A greater proportion of research is funded by commercial sponsors . IRBs feel pressure to accommodate these sponsors who are looking for quick turnaround ...
... increasing cost pressures due to the rise of managed care and capitated payments . A greater proportion of research is funded by commercial sponsors . IRBs feel pressure to accommodate these sponsors who are looking for quick turnaround ...
Page 18
... increases of 42 percent in initial reviews during the past 5 years at the sites we visited . Some of them are now reviewing more than 2,000 protocols annually . These IRBs are also being flooded with adverse - event reports from the ...
... increases of 42 percent in initial reviews during the past 5 years at the sites we visited . Some of them are now reviewing more than 2,000 protocols annually . These IRBs are also being flooded with adverse - event reports from the ...
Page 19
... increased workload , coupled with resource constraints , causes problems for IRBs and threatens the adequacy of their ... increase the length of their meetings , but many others are forced to squeeze more reviews into a fixed block of ...
... increased workload , coupled with resource constraints , causes problems for IRBs and threatens the adequacy of their ... increase the length of their meetings , but many others are forced to squeeze more reviews into a fixed block of ...
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amphetamine approved asked assurance BARRETT behavior Belmont Report benefits Biological Psychiatry biomedical Center Chairman Christopher Shays clinical research clinical trials Committee concerns conducted consent form continuing review disorders drug ELLIS ensure ethical evaluate Federal regulations Fen-Phen fenfluramine fenfluramine study funded Government Reform GROB haloperidol Health and Human HIMA Human Services human subject protection human subjects research informed consent document informed consent process Institutional Review Boards investigators IRB members IRB process IRB review IRB system IRB's issues June 11 Kammen DP KUCINICH Levine MESLIN methylphenidate monitoring NBAC NIH-GRANT-NUMBER NIH/OPRR NIMH Nuremberg Code Office OIG's OPRR patients pharmaceutical population potential problems procedures Protection from Research protection of human Psychiatric Institute Psychopharmacology question recommendations recruited Reform and Oversight regulatory require research protocols Research Risks research subjects response schizophrenia scientific serotonin SHAYS SNOWBARGER sponsors staff Thank Timothy Walsh Towns understand volunteer WALSH YESSIAN
Popular passages
Page 44 - ... injury occurs and, if so, what they consist of, or where further information may be obtained 7. An explanation of whom to contact for answers to pertinent questions about the research and research subjects' rights, and whom to contact in the event of a research-related injury to the subject 8.
Page 43 - A statement that the study involves research, an explanation of the purposes of the research and the expected duration of the subject's participation, a description of the procedures to be followed, and identification of any procedures which are experimental...
Page 44 - A statement describing the extent, if any, to which confidentiality of records identifying the subject will be maintained; (6) For research involving more than minimal risk, an explanation as to whether any compensation and an explanation as to whether any medical treatments are available if injury occurs and, if so, what they consist of, or where further information may be obtained; (7) An explanation of whom to contact for answers to pertinent questions about the research and research subjects'...
Page 42 - When some or all of the subjects are likely to be vulnerable to coercion or undue influence, such as children, prisoners, pregnant women, mentally disabled persons, or economically or educationally disadvantaged persons, additional safeguards have been included in the study to protect the rights and welfare of these subjects.
Page 45 - Department of Agriculture Department of Commerce Department of Defense Department of Education Department of Energy Department of Health and Human Services Department of Housing and Urban Development...
Page 123 - New imaging techniques, such as positron emission tomography (PET) and functional magnetic resonance imaging (fMRI), promise advances in our ability to identify regions of the brain associated with cognitive and affective disorders.
Page 144 - This meeting is adjourned. [Whereupon, at 3:35 pm, the subcommittee was adjourned, to reconvene at the call of the Chair.] [Additional information submitted for the hearing record follows:] EXECUTIVE OFFICE OF THE PRESIDENT OFFICE OF MANAGEMENT AND BUDGET WASHINGTON.
Page 4 - ... opening statement in the record, and that the record remain open for 3 days for that purpose. Without objection, so ordered. I ask further unanimous consent that all witnesses be permitted to include their written statements in the record.
Page 43 - ... a description of the procedures to be followed, and identification of any procedures which are experimental; (2) A description of any reasonably foreseeable risks or discomforts to the subject...
Page 40 - Ideally, it is a local review, by individuals who are in the best position to know the resources of the institution, the capabilities and reputations of the investigators and staff, and the prevailing values and ethics of the community and likely subject population.