Institutional Review Board (IRB)
GPTKB entity
Statements (48)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:Ethics
gptkb:government_agency |
| gptkbp:abbreviation |
gptkb:IRB
|
| gptkbp:approvedBy |
research involving human participants
|
| gptkbp:canBe |
suspend research
terminate research disapprove research require modifications to research protocols |
| gptkbp:countryOfOrigin |
gptkb:United_States
|
| gptkbp:establishedBy |
gptkb:National_Research_Act_of_1974
|
| gptkbp:existsIn |
gptkb:government_agency
hospitals universities private companies research institutions |
| gptkbp:guarantees |
compliance with regulations
ethical standards |
| https://www.w3.org/2000/01/rdf-schema#label |
Institutional Review Board (IRB)
|
| gptkbp:language |
English
|
| gptkbp:meetingPlace |
at least once per year
|
| gptkbp:must_include |
gptkb:scientist
community members non-scientists |
| gptkbp:oversees |
clinical trials
|
| gptkbp:provides |
continuing review
|
| gptkbp:purpose |
protect rights and welfare of human research subjects
|
| gptkbp:regulates |
gptkb:Food_and_Drug_Administration
gptkb:U.S._Department_of_Health_and_Human_Services human subjects research |
| gptkbp:relatedTo |
gptkb:philosophy
gptkb:Common_Rule gptkb:Belmont_Report bioethics medical research human subject protection |
| gptkbp:requires |
gptkb:United_States_federal_law
federally funded research FDA-regulated research |
| gptkbp:reviewedBy |
privacy protections
research protocols vulnerable populations informed consent documents risk/benefit analysis |
| gptkbp:sometimesCalled |
Ethics Review Board (ERB)
Independent Ethics Committee (IEC) Research Ethics Board (REB) |
| gptkbp:bfsParent |
gptkb:Research_Ethics_Board
|
| gptkbp:bfsLayer |
7
|