The collection consists of audiovisual recordings related to bioethics, the bulk of which are recordings of lectures delievered at the Kennedy Institute of Ethics (KIE). This includes the KIE's Intensive Bioethics Courses and Advanced Bioethics Courses. The recordings are in a variety of formats, including audio cassettes, compact discs, DVDs, micro cassettes, VHS cassette tapes, 1/4" open reel audio, and other formats.
The National Bioethics Advisory Commission (NBAC) was established by President Bill Clinton in October 1995. This collection contains meeting materials and reports produced by NBAC, as well as the Commission's website.
The collection consists of papers presented at the Choices on our Conscience International Symposium on Human Rights, Retardation and Research, as well as the symposium's program.. The symposium was sponsored by the Joseph P. Kennedy Jr. Foundation and held in October 1971.
The collection contains documents related to U.S. bioethics commissions and other federal agencies that belonged to Barbara F. Mishkin. This includes the National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research, the Ethics Advisory Board, the President’s Commission for the Study of Ethical Problems in Medicine and Biomedical and Behavioral Research Records, and the Office of Technology Assessment.
The collection consists of materials on library ethics and medical experimentation on prisoners created by Mary Lee Bundy. Bundy (1927-1987) was a professor at the University of Maryland, College Park, College of Library and Information Services. She was also one of the officers of Urban Information Interpreters, Inc., a non-profit organzation that sought to make information services accessible to the urban poor.
The collection consists of the proceedings of meetings held by the National Institute of Health's Human Embryo Research Panel, dating from February 1994 to June 1994. The Human Embryo Research Panel was established to provide the Director of the National Institutes of Health (Harold Varmus) with recommendations regarding human embryo research and guidelines for federal funding of such research.
The collection contains materials for the NIH's Ethical and Regulatory Aspects of Human Subject Research course. It includes the syllabus and the readings for the course. The course was presented by the the NIH's Department of Clinical Bioethics at the Warren G. Magnuson Clinical Center from October-November 2002.
The collection consists of materials for the Ancillary-Care Obligations of Medical Researchers Working in Developing Countries Workshop (October 2006). The workshop was sponsored by Georgetown University's Reflective Engagement Initiative with additional support from the University's Department of Philosophy, the Kennedy Institute of Ethics, and from the PhRMA Foundation. Materials include schedules, biographies, and handouts.
The collection documents the work of the Advisory Committee on Human Radiation Experiments (ACHR). It includes meeting briefing books, drafts of the final report and related records, background materials on experiments, and correspondence of ACHR Executive Director Dan Guttman. Meetings were held between 1994 and 1995, and the collection includes copies of background materials dating back to 1900.
The collection consists of three scrapbooks of clippings relating to the Kennedy Institute of Ethics, dating from 1971-1974.
The collection consists of the records of the Georgetown Ignatian Society and documents their efforts to have Georgetown University formally declared "un-Catholic" for their recognition of a pro-choice student group (GU Choice) and other offenses in the 1990s. It consists of their Petition to Cardinal Hickey, their Canon Law suits, correspondence, newspaper clippings, and anti-GU Choice buttons.
The collection consists of records related to the Biomedical Ethics Advisory Committee (BEAC). BEAC was formed in 1987 to counsel the congressional members of the national Biomedical Ethics Board on ethical issues that arise in the delivery of healthcare and biomedical research.
The Human Fetal Tissue Transplantation Research Panel was established in 1988 as an ad hoc consultant group to the Advisory Committee of to the Director of the National Institute of Health. The collection contains records related to the Panel, including meeting transcripts, briefing books, clippings, the Research Panel's final report, and other documents.
The collection consists of records of the U.S. Department of Health, Education, and Welfare's Ethics Advisory Board, which existed from 1978 to 1979.
The collection consists of statistical summary data for sixteen countries derived from a survey on ethical problems faced by medical geneticists. The survey was conducted by John C. Fletcher of the National Institutes of Health in 1986. The data was used in a study published in 1989 as Ethics and Human Genetics: A Cross-Cultural Perspective. The collection also includes an explanatory letter and a copy of the questionnaire.
