Institutional Review Boards (IRBs)
GPTKB entity
Properties (61)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
Ethics committee
|
| gptkbp:adaptedInto |
emerging ethical issues
|
| gptkbp:can_be |
research studies
independent centralized institutional waivers for consent |
| gptkbp:challenges |
research participants
|
| gptkbp:collaborates_with |
other IRBs
|
| gptkbp:composedOf |
diverse professionals
scientists non-scientists |
| gptkbp:defeated |
research activities
|
| gptkbp:ensures |
ethical standards in research
equitable treatment of participants |
| gptkbp:established |
U.S._federal_regulations
|
| gptkbp:evaluates |
vulnerable populations
confidentiality measures risk versus benefit |
| gptkbp:facilitates |
community engagement in research
research compliance |
| https://www.w3.org/2000/01/rdf-schema#label |
Institutional Review Boards (IRBs)
|
| gptkbp:includes |
community members
legal experts ethicists |
| gptkbp:influence |
research design
|
| gptkbp:influenced |
institutional policies
|
| gptkbp:is_a_route_for |
conduct continuing review
document their decisions review conflicts of interest |
| gptkbp:is_a_subject_of |
federal oversight
|
| gptkbp:is_essential_for |
ethical research practices
research integrity public trust in research human subject protection |
| gptkbp:is_governed_by |
the Common Rule
|
| gptkbp:is_involved_in |
policy development
adverse event reporting data safety monitoring research ethics training |
| gptkbp:is_part_of |
the research process
|
| gptkbp:monitors |
ongoing research
|
| gptkbp:protectedArea |
the rights of participants
|
| gptkbp:provides |
educational resources
consultation services guidance on ethical issues support for researchers resources for compliance feedback to researchers |
| gptkbp:regulates |
research involving human subjects
|
| gptkbp:regulatoryCompliance |
exempt research
|
| gptkbp:requires |
informed consent
annual reviews federally funded research additional safeguards protocol submissions |
| gptkbp:reviews |
research proposals
informed consent documents |
| gptkbp:suitableFor |
clinical trials
behavioral research social science research |