| IRB |
A committee designated by an institution, such as a hospital, to review and approve research projects; eg, clinical studies in that institution.
출처: www.condell.org/libertyville/neurosurgery/neurolog...
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| IRB |
In the US a group of scientists, doctors, clergy, and consumers at each health care facility that participates in a clinical trial. IRBs are designed to protect study participants. They review and must approve the action plan for every clinical trial. They check to see that the trial is well designed, does not involve undue risks, and includes safeguards for patients.
출처: www.iffgd.org/GIDisorders/glossary.html
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| IRB |
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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| IRB |
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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| IRB |
Immigration and Refugee Board
출처: www.psc-cfp.gc.ca/centres/definitions_and_notes_e....
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