The collection consists of records related to the President's Biomedical Research Panel (PBRP), including its final report (with Appendix A and C), the Analysis of Selected Biomedical Research Programs (2 volumes), and summary meeting minutes (1975-1976). The records belonged to Kathryn Arnow, who was a health policy analyst and Chief of the Program Planning Branch in the office of the Director of the National Institutes of Health in the 1970s.
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 primarily consists of interviews conducted by James H. Jones with medical professionals who were responsible for the care of David Vetter. Vetter suffered from severe combined immunodeficiency (SCID) and was popularly known as the "Bubble Boy." The interviews were conducted in 2001 for a book that was ultimately not completed. Additionally, the collection contains audiovisual materials and photographs related to Vetter.
The collection contains the papers of Dr. Edmund D. Pellegrino, dating from 1943 to 2017. It primarily documents his contributions to the field of bioethics, particuarly as an educator and administrator at Georgetown University.
The collection documents 43 meetings of the National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research held between 1974 and 1978 and includes briefing books, subject files, and transcripts from these meetings. The Executive’s Branch of the Department of Health, Education, and Welfare established the group in 1974 and it is considered one of the first modern bioethics commissions.
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 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 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 consists of records related to the National Heart Transplantation Study, including the project proposal, advisory committee meeting minutes, a description of the study (with selected readings), published updates, questionnaires, and forms. It also includes forms related to the National Kidney Dialysis and Transplantation Study.
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 Pellegrino Center for Clinical Bioethics Records primarily consist of conference, meeting, and event files. They also include annual reports, newsletters, budget files, and reports. In addition to documents, the records include photographs and computer disks that contain digital images and audio recordings (MP3).
