| IRB |
An independent group of professionals designated to review and approve the clinical protocol, Informed Consent Forms, study advertisements, and patient brochures to ensure that the study is safe and effective for human participation. The IRB also ensures that the study adheres to FDA regulations.
출처: www.dcri.duke.edu/patient/glossary.jsp
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| IRB |
a panel at each institution doing research on human subjects that reviews the risks posed to subjects and the consent process proposed
출처: www.mywhatever.com/cifwriter/content/66/4620.html
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| IRB |
An IRB is the group or committee that is given the responsibility by an institution to review that institution's research projects involving human subjects. The primary purpose of the IRB review is to assure the protection of the safety, rights and welfare of the human subjects. At the University of Washington, the IRB is called the "Human Subjects Review Committee."
출처: www.washington.edu/healthresearch/definitions.html
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| IRB |
A group of doctors, scientists, lawyers, community members, and patient advocates appointed by a medical institution who are responsible for reviewing and approving research studies that involve humans. IRBs assure that such studies are scientifically and ethically proper to conduct.
출처: www.jhu.edu/wctb/coms/booklet/book5.htm
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| IRB |
Under the Common Rule, a local review board convened by any institution conducting federally sponsored human subject research, vested with the responsibility to review research proposals to ensure compliance with federal research regulations.
출처: www.eh.doe.gov/ohre/roadmap/achre/glossary.html
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