International Compilation of Human Research Protections, 2008 edition
United States. Department of Health and Human Services. Office of Human Research Protections [OHRP]
Rockville, MD: Office of Human Research Protections [OHRP], 2008: 75 p. [Online]. Accessed: http://www.hhs.gov/ohrp/international/HSPCompilation.pdf [2008 February 12]
Research; Confidentiality; Drugs and Drug Industry; Cloning; Genetics, Molecular Biology and Microbiology; Human Experimentation Policy Guidelines / Institutional Review Boards; Informed Consent or Human Experimentation; Donation / Procurement of Organs and Tissues; International and Political Dimensions of Biology and Medicine; Research on Embryos and Fetuses;
Showing items related by title, author, creator and subject.
Unknown author (United States. Department of Health and Human Services [HHS]. Office for Human Research Protections [OHRP], 2005-10-01)
Department of Health and Human Services. Food and Drug Administration. Regulations Requiring Manufacturers to Assess the Safety and Effectiveness of New Drugs and Biological Products in Pediatric Patients Letter and Attachment From Robert P. Murphy, General Counsel, United States General Accounting Office to Sen. James M. Jeffords and Sen. Edward M. Kennedy and Rep. Thomas J. Bliley, Jr. and Rep. John D. Dingell Murphy, Robert P. (United States. General Accounting Office [GAO], 1998-12-21)
United States. Department of Health and Human Services [HHS]. Office for Human Research Protections [OHRP] (2009-12)