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A quick check of your next patient chart shows a woman with irregular or absent ovulation and elevated levels of androgenic hormones. Whats your initial diagnosis?
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Wilke AJ. News Briefs. Altern Ther Women's Health 2004;6(8):64.
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To clinical trial coordinators looking for study subjects, a nearby university campus looks like a godsend large numbers of unemployed young people all in one place for a designated period of time.
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So what should an advertisement recruiting trial subjects say? W. Parker Nolen, MBA, IRB administrator for St. Josephs Hospital in Atlanta, recommends the following:
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IRBs are not required to review stand-alone HIPAA waivers as part of their oversight of research subject protections even if their written policies and procedures indicate they will review any written documentation provided to potential study participants, the U.S. Food and Drug Administration (FDA) clarified in a recent guidance document issued Oct. 21, 2003, and published in the Nov. 7 issue of the Federal Register.
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Its pretty much a given that computer-based recordkeeping will play a part in a clinical trial.
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A recent study by the Maternal & Child Health Policy Research Center makes clear that when it comes to caring for adolescents, the health care system is not doing a very good job.
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More than two years after the terrorist attacks in New York City and Washington, DC, and despite $1.8 appropriated by Congress to revitalize the countrys public health system, some progress has been made, but not nearly enough, according to a report prepared by Trust for Americas Health.
