Medical Ethics
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IRB Continuing Education Series Turns Students into Teachers
Newark, DE-based Christiana Care Health System’s long-time educational program was set up to keep research nurses up to date, but over time it lost its luster.
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Smart Training Can Prevent Problems with New Technology
Adopting new electronic submission technology across a research enterprise organization can prove to be challenging for IRBs, which have a long list of stakeholders to train and educate.
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Some Spit, Polish, and Creativity Can Solve IRBs’ Education Efforts
IRB leaders at Christiana Care Health System in Newark, DE, revamped their research education sessions in response to dwindling attendance numbers.
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Transparency About Participation Incentives Could Benefit IRBs, Researchers, and Patients
While the issue of incentives raises a host of ethical issues for discussion, the problem is the dearth of data on what study participants have been compensated for all manner of studies and clinical trials.
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What You Don’t Know About NIH RAC Review Changes Could Hurt
IRBs might not have asked for it, but the National Institutes of Health and the FDA have handed them a new responsibility when it comes to oversight of clinical trials involving human gene transfer.
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Who was Dan Markingson?
On May 8, 2004, Dan Markingson killed himself while participating in a University of Minnesota Department of Psychiatry drug study.
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U. of Minnesota Fights Bill Giving State Oversight of Psych Research
Reeling from a decade-long series of investigations and allegations after the suicide of a psychiatric research patient, the University of Minnesota is now facing a proposed state law that would assign oversight for its psychiatric drug research program to an independent ombudsman’s office.
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Ethics tool could enhance protocols and subject protection
A multiple stakeholder group developed a protocol ethics tool kit to ensure there is no missing information regarding ethics considerations in protocols.
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‘Optimistic bias’ may subvert informed consent in early-phase cancer trials
There is a gray area where optimism in a research patient in early phase cancer trials crosses over to a misperception of benefit and raises ethical questions about informed consent.
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Maryland Gets a New View of Conflicts of Interest
An investigative committee at the University of Maryland in College Park recommends mandatory education on conflicts of interest for research faculty.