# OnCo record ethics-review (term). Data CC BY-NC 4.0, attribute "Data from OnCo (onco.cc)". Whole corpus: https://onco.cc/api/v1/onco.nt
@prefix schema: <https://schema.org/> .
@prefix onco: <https://onco.cc/ns#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .

<https://onco.cc/terms/ethics-review/>
  a schema:DefinedTerm ;
  onco:kind "term" ;
  schema:identifier "ethics-review" ;
  schema:name "Ethics review (IRB, research ethics committee)"@en ;
  schema:alternateName "ethics review"@en, "ethical review"@en, "ethics committee"@en, "ethics committees"@en, "research ethics committee"@en, "research ethics committees"@en, "REC"@en, "institutional review board"@en, "institutional review boards"@en, "IRB"@en, "IRBs"@en, "IRB approval"@en, "ethics approval"@en, "ethical approval"@en, "approved by the ethics committee"@en, "central IRB"@en, "single IRB"@en, "local IRB"@en, "independent ethics committee"@en, "IEC"@en, "Declaration of Helsinki"@en, "Belmont Report"@en, "Common Rule"@en, "45 CFR 46"@en, "Good Clinical Practice"@en, "GCP"@en, "ICH E6"@en, "vulnerable participants"@en, "minimal risk"@en, "risk-benefit assessment"@en, "protocol review"@en, "continuing review"@en, "annual review"@en, "serious breach"@en, "protocol violation"@en ;
  schema:description "Before a trial can enrol anyone, an independent ethics committee (an IRB in the United States, a research ethics committee in the United Kingdom) reviews the protocol and the consent form to decide whether the risks are justified and the participants are protected, and it keeps watching until the trial ends."@en ;
  schema:url <https://onco.cc/terms/ethics-review/> ;
  schema:dateModified "2026-09-17"^^xsd:date ;
  schema:sameAs <https://en.wikipedia.org/wiki/Institutional_review_board> ;
  schema:citation <https://en.wikipedia.org/wiki/Institutional_review_board>, <https://www.hhs.gov/ohrp/regulations-and-policy/regulations/45-cfr-46/index.html>, <https://www.wma.net/what-we-do/medical-ethics/declaration-of-helsinki/>, <https://www.ich.org/page/efficacy-guidelines> ;
  onco:related <https://onco.cc/terms/informed-consent/>, <https://onco.cc/terms/clinical-equipoise/>, <https://onco.cc/terms/data-monitoring-committee/>, <https://onco.cc/terms/trial-protocol/>, <https://onco.cc/terms/trial-lifecycle/>, <https://onco.cc/terms/trial-registration/>, <https://onco.cc/terms/accrual/>, <https://onco.cc/terms/regulatory-agencies/> ;
  onco:sections <https://onco.cc/fronts/drug-discovery/> ;
  onco:trials <https://onco.cc/trials/low-dose-nivolumab-tmh/>, <https://onco.cc/trials/olanzapine-appetite-tmh/>, <https://onco.cc/trials/kerala-oral-screening/> .