Search Results Search Sort by RelevanceMost Recent History of Medicine Aug 2006 Lessons in Dermatology Research: Protecting Vulnerable Research Participants T. Howard Stone, JD, LLM Virtual Mentor. 2006;8(8):533-537. doi: 10.1001/virtualmentor.2006.8.8.mhst1-0608. State of the Art and Science May 2018 Defining “Community” and “Consultation” for Emergency Research that Requires an Exception from Informed Consent Samuel A. Tisherman, MD Emergency research that requires exception from informed consent presents challenges in defining and reaching the at-risk community. AMA J Ethics. 2018;20(5):467-474. doi: 10.1001/journalofethics.2018.20.5.stas1-1805. In the Literature Aug 2009 The Belmont Report's Misleading Conception of Autonomy Sigurdur Kristinsson, PhD Virtual Mentor. 2009;611-616. doi: 10.1001/virtualmentor.2009.11.8.jdsc1-0908. Health Law Nov 2004 Wright v. Fred Hutchinson Cancer Center: Maintaining Patient and Public Trust in Clinical Research Laura Lin, MBA and Bryan A. Liang, MD, PhD, JD Virtual Mentor. 2004;6(11):501-504. doi: 10.1001/virtualmentor.2004.6.11.hlaw1-0411. Health Law Nov 2003 Grimes v. Kennedy Krieger Institute: Nontherapeutic Research with Children Richard Morse, MA Virtual Mentor. 2003;5(11):503-507. doi: 10.1001/virtualmentor.2003.5.11.hlaw1-0311. Medicine and Society Nov 2004 Gatekeeping and the FDA's Role in Human Subjects Protection Daniel Carpenter, PhD Virtual Mentor. 2004;6(11):512-514. doi: 10.1001/virtualmentor.2004.6.11.msoc1-0411. Policy Forum Apr 2009 The History and Role of Institutional Review Boards: A Useful Tension Margaret R. Moon, MD, MPH Institutional review boards (IRBs) play a role in approving research that involves human subjects. Virtual Mentor. 2009;11(4):311-316. doi: 10.1001/virtualmentor.2009.11.4.pfor1-0904. Health Law Apr 2009 Institutional Review Board Liability for Adverse Outcomes Micah R. Onixt, JD and Robyn L. Sterling, JD, MPH Institutional review boards (IRBs) have the responsibility to ensure the protection of human-research subjects and are legally liable if they fail to do so. Virtual Mentor. 2009;11(4):306-310. doi: 10.1001/virtualmentor.2009.11.4.hlaw1-0904. Policy Forum Apr 2009 The History and Role of Institutional Review Boards: Local and Central IRBs, A Single Mission Felix Khin-Maung-Gyi, PharmD, MBA Institutional review boards (IRBs) play a role in approving research that involves human subjects. Virtual Mentor. 2009;11(4):317-321. doi: 10.1001/virtualmentor.2009.11.4.pfor1-0904. In the Literature Jul 2009 Clinical Research in Low- and Middle-Income Countries Mark Boyd, MD, FRACP There are advantages and objections to conducting clinical trials in middle-income nations and possible approaches to overcoming the objections. Virtual Mentor. 2009;11(7):511-515. doi: 10.1001/virtualmentor.2009.11.7.jdsc1-0907. Pagination Current page 1 Page 2 Next page Next › Last page Last »
History of Medicine Aug 2006 Lessons in Dermatology Research: Protecting Vulnerable Research Participants T. Howard Stone, JD, LLM Virtual Mentor. 2006;8(8):533-537. doi: 10.1001/virtualmentor.2006.8.8.mhst1-0608.
State of the Art and Science May 2018 Defining “Community” and “Consultation” for Emergency Research that Requires an Exception from Informed Consent Samuel A. Tisherman, MD Emergency research that requires exception from informed consent presents challenges in defining and reaching the at-risk community. AMA J Ethics. 2018;20(5):467-474. doi: 10.1001/journalofethics.2018.20.5.stas1-1805.
In the Literature Aug 2009 The Belmont Report's Misleading Conception of Autonomy Sigurdur Kristinsson, PhD Virtual Mentor. 2009;611-616. doi: 10.1001/virtualmentor.2009.11.8.jdsc1-0908.
Health Law Nov 2004 Wright v. Fred Hutchinson Cancer Center: Maintaining Patient and Public Trust in Clinical Research Laura Lin, MBA and Bryan A. Liang, MD, PhD, JD Virtual Mentor. 2004;6(11):501-504. doi: 10.1001/virtualmentor.2004.6.11.hlaw1-0411.
Health Law Nov 2003 Grimes v. Kennedy Krieger Institute: Nontherapeutic Research with Children Richard Morse, MA Virtual Mentor. 2003;5(11):503-507. doi: 10.1001/virtualmentor.2003.5.11.hlaw1-0311.
Medicine and Society Nov 2004 Gatekeeping and the FDA's Role in Human Subjects Protection Daniel Carpenter, PhD Virtual Mentor. 2004;6(11):512-514. doi: 10.1001/virtualmentor.2004.6.11.msoc1-0411.
Policy Forum Apr 2009 The History and Role of Institutional Review Boards: A Useful Tension Margaret R. Moon, MD, MPH Institutional review boards (IRBs) play a role in approving research that involves human subjects. Virtual Mentor. 2009;11(4):311-316. doi: 10.1001/virtualmentor.2009.11.4.pfor1-0904.
Health Law Apr 2009 Institutional Review Board Liability for Adverse Outcomes Micah R. Onixt, JD and Robyn L. Sterling, JD, MPH Institutional review boards (IRBs) have the responsibility to ensure the protection of human-research subjects and are legally liable if they fail to do so. Virtual Mentor. 2009;11(4):306-310. doi: 10.1001/virtualmentor.2009.11.4.hlaw1-0904.
Policy Forum Apr 2009 The History and Role of Institutional Review Boards: Local and Central IRBs, A Single Mission Felix Khin-Maung-Gyi, PharmD, MBA Institutional review boards (IRBs) play a role in approving research that involves human subjects. Virtual Mentor. 2009;11(4):317-321. doi: 10.1001/virtualmentor.2009.11.4.pfor1-0904.
In the Literature Jul 2009 Clinical Research in Low- and Middle-Income Countries Mark Boyd, MD, FRACP There are advantages and objections to conducting clinical trials in middle-income nations and possible approaches to overcoming the objections. Virtual Mentor. 2009;11(7):511-515. doi: 10.1001/virtualmentor.2009.11.7.jdsc1-0907.