| institutional review board |
An independent committee of doctors, scientists, clergy, and health care consumers located at the institution where a clinical trial is to take place. The IRB reviews the trial to make sure it is ethical and protects the rights and safety of study participants. IRBs approve and monitor almost all clinical trials in the United States.
출처: www.melanomacenter.org/glossary/i.html
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| institutional review board |
A group that reviews studies proposed by investigators. Each institution that conducts research has an IRB made up of researchers and members of the public. The IRB must be sure that the study is managed in a way that protects those who participate in it.
출처: www.mayoclinic.com/invoke.cfm
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| institutional review board |
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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| institutional review board |
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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| institutional review board |
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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