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VA mandates review of research programs; Partial-birth abortion ban approved by Senate.
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Patients with severe, irreversible brain injuries present unique ethical challenges to physicians and hospital ethics committees. For patients with no chance of recovering an interactive, conscious state, which treatments are appropriate and which are unjustifiably invasive and pointless?
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Nearly every hospital has them, and most doctors have seen them, treated them, and agonized over them. They are patients with a slim, if not nonexistent, chance of recovery, who continue to receive intense, invasive, and costly procedures because there is no other clear alternative.
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The Department of Veterans Affairs (VA) last month issued a nationwide ultimatum to its medical centers involved in research to shape up or else.
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The Baylor College of Medicine in Houston has a prescribed inquiry process for complaints generated by human subject research at the institution, says Kathleen Motil, PhD, MD, associate professor of pediatrics and chair of two of the colleges IRBs.
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Two years ago, Baylor College of Medicine had a dilemma: double its staff to accommodate the increase in study protocols being submitted to its IRB or find an electronic solution to its problem. They chose the latter.
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While the Health Insurance Portability and Accountability Act of 1996 (HIPAA) is clearly getting all the headlines and a great deal of attention in the research community, the recent Food and Drug Administration (FDA) Guidance for Industry on Electronic Records indicates it is not the only game in town.
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As genetics research yields more and more information about individuals predispositions to disease and illness, researchers are beginning to question whether study participants should have access to the genetic information obtained about them.
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