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To better clarify the IRBs position in investigating clinical investigators and sites for clinical trials, the Food and Drug Administration (FDA) has released draft guidance for reviewing those qualifications.
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The University of California at Berkeleys Consent Builder application relies on the simplified language and template structure previously developed by the institutions IRB office.
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Sometimes an IRB director will notice that board members lack interest in evaluation processes. Any attempt to assess how each member is doing might be shuffled to the back burner of the schedules of very busy people.
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A new research ethics program seeks to repair problems when investigators misbehave or are in noncompliance.
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The American Association of University Professors (AAUP) released a report taking IRBs to task over what they call inappropriate, indeed absurd, alterations in research protocols and overly stringent guidelines for study submission and approval.
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Years of improvements to the informed consent process and many hours of developing tools and templates to assist IRBs and investigators in fine tuning informed consent documents have helped pave the way for Consent Builder.
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While monstrous hurricanes are not a frequent occurrence, it always pays to be prepared. Hurricane Sandy was something of an anomaly, but cities and hospitals in the Northeast braced for the monster hurricane, putting plans in place to evacuate patients when needed and ways to continue operations even if the worst happened.
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Get ready, IRBs data collection for financial conflicts of interest (FCOIs) is about to get more complicated.
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The University of California Los Angeles (UCLA) recently updated its guidance on reporting unanticipated problems (UPs), adverse events (AEs), and other incidents in human subject research, providing a model for IRBs.
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The IRB office at the University of Utah in Salt Lake City takes its standard operating procedures (SOPs) very seriously. The IRB even dedicates one highly experienced, part-time professional to make frequent revisions and improvements to the SOPs and guidance.