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Full-Text Articles in Law
Mid-Atlantic Ethics Committee Newsletter, Summer 2003
Mid-Atlantic Ethics Committee Newsletter, Summer 2003
Mid-Atlantic Ethics Committee Newsletter
No abstract provided.
Mid-Atlantic Ethics Committee Newsletter, Spring 2003
Mid-Atlantic Ethics Committee Newsletter, Spring 2003
Mid-Atlantic Ethics Committee Newsletter
No abstract provided.
Regulating Clinical Research: Informed Consent, Privacy, And Irbs, Sharona Hoffman
Regulating Clinical Research: Informed Consent, Privacy, And Irbs, Sharona Hoffman
Faculty Publications
During the past two decades, the United States has experienced dramatic developments in the area of biomedical research. Expanding budgets, augmented computer capabilities, and the Human Genome Project have all significantly enhanced research capabilities. Consequently, the number of research projects conducted in this country is ever growing, and the enrollment of an adequate number of human subjects is becoming an increasingly challenging task.
Clinical research involving human participants is governed by federal regulations that have been promulgated by the Department of Health and Human Services (DHHS) and the Food and Drug Administration (FDA). In light of the proliferation of medical …