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Everyone does more work with less time these days. So how can an IRB make new board member training effective without being time demanding? One IRB has found that the answer is to hold brief educational sessions during its board meetings.
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Human research protection program staff at the VA Medical Center in Tuscaloosa, AL, knew there was a problem with the IRB's expedited review process.
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[Editor's note: Valerie Bonham, JD, executive director of the Presidential Commission for the Study of Bioethical Issues, answers these two questions about the new International Research Panel formed this year by President Barack Obama.]
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When consultant Jeffrey Cooper talks to IRBs about using the flexibility of federal regulations to change their procedures, he can see that the message doesn't always get through.
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Five years ago, a panel of researchers and others involved in social and behavioral sciences convened to explore concerns about the scope and effectiveness of IRB review.
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How do you bridge the gap between an IRB that believes all of the work you do is subject to oversight and a faculty that thinks none of it is?
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When a researcher breaches a cultural divide to study a group of people, he or she needs more than a translator to convert documents from one language to another.
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In July 2011, Joint Commission (JC) surveyors will begin holding hospitals accountable for some of the elements of performance (EP) contained in new patient-centered communication standards that were first unveiled last summer.
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