Articles Tagged With: IRB
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Researchers Encounter Challenges with Study Development Protocols
Tutorial videos and webinars, in-person training, and sample forms are some of the ways researchers try to keep up with IRB protocols to prevent any study delays.
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Framework for Developing Health Research Ethics Competencies
Researchers were surprised that despite ongoing efforts to develop research ethics programs over many years in the United States and internationally, there was no published competency framework to follow, nor was there a standard approach to creating competencies in this context. This, despite the fact competencies have been used for education in business, medicine, and elsewhere for decades. -
IRB Staff Training Program Improves Consistency and Work Group Efficiency
When an IRB office aimed to improve its staff training and work efficiency, the solution was to create a new program, called the IRB Staff Training and Onboarding Program. The process began with the IRB’s internal staff training and member work group and leaders identifying ways to improve training and onboarding of new IRB staff. -
Take Steps to Prevent Damaging Security Breaches in Survey Studies
IRBs can help investigators create a plan to prevent survey security breaches that can lead to false data and study slowdowns and shutdowns. IRBs should ensure researchers know that if they detect a breach that changes/corrupts data, leads to someone outside the research team accessing data, causes potential harm to participants, or requires a change in procedures or informed consent, it should be reported to the IRB.
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U.K. Approves First COVID-19 Human Challenge Trial
Volunteers will be infected with virus so researchers can learn more about pathology, speed effective vaccine development.
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IRB Reduces Student Study Review Time from 65 Days to 8 Days
It is possible to shorten IRB review time dramatically, but it requires some resources and time. The IRB of Northcentral University serves a nontraditional population of students, some of whom want to complete a research study as part of their academic plan. The IRB’s streamlining process reduced the submission-to-approval time to eight days, down from an average of 65 days before the new process, according to new, unpublished data.
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Study Shows Research Programs and IRBs Responded Quickly to the Pandemic
Human research protection programs and IRBs nationwide responded quickly and efficiently to changing processes and policies during the early months of the COVID-19 pandemic, according to the results of a recent study.
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Cheap, Common Steroid Shows Efficacy Against COVID-19
British researchers are excited about their discovery, but full results have not been published.
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Research Organizations Face Challenges New and Old
As current studies resume and new studies are approved, IRBs and researchers should keep basic safety and regulatory practices in mind, according to experts on the front lines of human research protection and clinical trials.
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Q&A Part 3: IRBs Learn Positive and Instructional Lessons from Pandemic
IRB experts share the ways in which the pandemic has spurred innovation in their institutions.