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The Office for Human Research Protections (OHRP) in Washington, DC, is indicating to research institutions that the agency favors the use of centralized IRBs for multisite studies.
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The Office for Human Research Protections (OHRP) in Washington, DC, recently published letters that explain the agency's revised stand on the use of central or external IRBs.
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Based on a survey of research participants, the office of research compliance and quality improvement at Cedars-Sinai Medical Center in Los Angeles, CA, has come up with these four key areas to demonstrate informed consent.
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When Vanderbilt University Medical Center set about creating its BioVU biobank, it went in a different direction than most institutions.
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Young black men are disproportionately more likely than other groups to be victims of violent crime. But when researchers set out to study this group, they encounter difficulty in recruiting and retaining subjects.
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Just as identify theft has been steadily increasing in the general populace, so has it grown in the medical setting, with the ED perhaps feeling the greatest impact of all.
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Several years ago the security plans for the ED at Miami Valley Hospital in Dayton, OH, were significantly revamped. The process required strong teamwork between ED leadership and hospital security.
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The practice of emergency medicine is unique in that an emergency medicine physician acts as a gatekeeper. While treatment of a patient might be brief, initial examination and assessment often will dictate the course of the patient's treatment after admission to the hospital.
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The Joint Commission has suspended its policy that triggers an "automatic" adverse decision if an organization fails to complete an acceptable root cause analysis in response to a sentinel event or its related measure of success within a specified time frame. The change is retroactively effective as of Jan. 1, 2010.