Human Radiation and Other Scientific Experiments: The Federal Government's Role : Hearing Before the Committee on Governmental Affairs, United States Senate, One Hundred Third Congress, Second Session, January 25, 1994 |
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Administration Advisory agencies Answer approval Army assurance Atomic Energy Belmont Report benefits cancer Chairman GLENN classified clinical trials cold war Committee compliance concerned conducted congenital CRAFT Defense Department of Energy disease documents dose drug ethical facilities Fernald School follow-up funded going Government Health and Human human experimentation human radiation experiments human research identify individuals informed consent Institutional Review Board Interagency Working Group investigations involving human subjects ionizing radiation isotope issues leukemia MASSÉ ment monitoring mothers nuclear medicine Nuremberg Code OPRR participants patients personnel plutonium population pregnancy pregnant women prenatal procedures protection of human Question radi radiation exposure radiation research radioactive iron radioisotope records regulations research subjects risk scientific Secretary BROWN Secretary O'LEARY Senator SASSER standards Thank tion tracer treatment U.S. Army Vanderbilt veterans
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Page 159 - Memorandum for Secretaries of the Military Departments, Chairman of the Joint Chiefs of Staff, Under Secretaries of Defense Director, Defense Research and Engineering, Assistant Secretaries of Defense, General Counsel of the Department of Defense.
Page 108 - It read, in part, that every human being of adult years and sound mind has a right to determine what shall be done with his own body; and a surgeon who performs an operation without his patient's consent commits an assault, for which he is liable in damages.
Page 166 - 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.
Page 107 - PHS agencies, including the National Institutes of Health, the Centers for Disease Control and Prevention, and the...
Page 148 - Suspension or termination of IRB approval of research. An IRB shall have authority to suspend or terminate approval of research that is not being conducted in accordance with the IRB's requirements or that has been associated with unexpected serious harm to subjects.
Page 109 - ... obtain the consent of such human beings or their representatives, except where they deem it not feasible or, in their professional judgment, contrary to the best interests of such human beings.
Page 114 - The department of medical zoology of the School of Hygiene and Public Health of the Johns Hopkins University...
Page 161 - ... detonations. (iv) The term onsite participation means: (A) During the official operational period of an atmospheric nuclear test, presence at the test site, or performance of official military duties in connection with ships, aircraft or other equipment used in direct support of the nuclear test. (B) During the six month period following the official operational period of an atmospheric nuclear test, presence at the test site or other test staging area to perform official military duties in connection...
Page 114 - I had applied the digestive medicament 27 feeling but little pain, their wounds neither swollen nor inflamed, and having slept through the night. The others to whom I had applied the boiling oil were feverish, with much pain and swelling about their wounds. Then I determined never again to burn thus so cruelly the poor wounded by arquebuses.
Page 167 - Each IRB shall include at least one member who is not otherwise affiliated with the institution and who is not part of the immediate family of a person who is affiliated with the institution.