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The newly accredited MaGil IRB in Rockville, MD, has review process timelines that might seem impossible to other organizations, including a self-imposed deadline of four hours from the time an IRB review submission is made to the time it is seen by IRB members.
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IRB staff professionals need a greater breadth of knowledge and training now than they might have a decade ago, which is why one HRPP recently created a more comprehensive educational program that also offers greater autonomy to staff.
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Just as companies are offering whole genome sequencing to individuals, companies are offering to sequence their microbiomes and determine how they compare to others.
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The Office of Human Research Protections (OHRP) and the Food and Drug Administration (FDA) encourage the use of the central IRB model to increase the efficiency and quality of multisite trials.
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The Office for Human Research Protections' 2014 Edition of International Compilation of Human Research Standards is available with hundreds of updates and three additional nations, including Cameroon, Mozambique, and Zambia.
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In their search for ways to improve informed consent, IRBs and the research community have used illustrations, different sizes and styles of fonts, simple language, videos, interactive displays, and other innovative methods.
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A large health system IRB found that incomplete study submissions were clogging up the IRB review system, resulting in long waits up to three months for approval.
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Academic and medical research institutions and their IRBs often have to deal with study proposals that fall between research and quality improvement (QI).
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Translation of full informed consent forms into other languages can be a costly and time-consuming endeavor for researchers, particularly if there are few non-English speaking participants in a study.