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- NCIT_C16468 IAO_0000115 "A document explaining all the relevant information to assist an individual in understanding the expectations and risks in making a decision about a procedure. This document is presented to and signed by the individual or guardian." @default.
- NCIT_C16468 NCIT_NHC0 "C16468" @default.
- NCIT_C16468 NCIT_P106 "Intellectual Product" @default.
- NCIT_C16468 NCIT_P108 "Consent Form" @default.
- NCIT_C16468 NCIT_P207 "C0009797" @default.
- NCIT_C16468 NCIT_P322 "CDISC" @default.
- NCIT_C16468 NCIT_P322 "CDISC-GLOSS" @default.
- NCIT_C16468 NCIT_P322 "CareLex" @default.
- NCIT_C16468 NCIT_P325 "A document to capture consent by a patient to a surgical or medical procedure or participation in a clinical study after achieving an understanding of the relevant medical facts and the risks involved. [NCI]" @default.
- NCIT_C16468 NCIT_P325 "A formal document used during the informed consent process explaining the potential risks and benefits of participation in a study and the rights and responsibilities of the parties involved, in a manner that is understandable to the subject or their legally authorized representative." @default.
- NCIT_C16468 NCIT_P325 "Document used during the informed consent process that is the basis for explaining, in understandable language, to potential subjects (or legally-authorized representative) the risks and potential benefits of a study and the rights and responsibilities of the parties involved. NOTE: The informed consent document provides a summary of a clinical trial (including its purpose, the treatment procedures and schedule, potential risks and benefits, alternatives to participation, etc.) and explains an individual's rights as a subject. [After FDA Informed Consent Information Sheet Guidance for IRBs, Clinical Investigators, and Sponsors, July 2014] See also informed consent." @default.
- NCIT_C16468 NCIT_P366 "Consent_Form" @default.
- NCIT_C16468 normalizedInformationContent "100" @default.
- NCIT_C16468 referenceCount "1" @default.
- NCIT_C16468 hasExactSynonym "Consent Form" @default.
- NCIT_C16468 hasExactSynonym "IC Form" @default.
- NCIT_C16468 hasExactSynonym "ICF" @default.
- NCIT_C16468 hasExactSynonym "Informed Consent Document" @default.
- NCIT_C16468 hasExactSynonym "Informed Consent Form" @default.
- NCIT_C16468 hasExactSynonym "consent form" @default.
- NCIT_C16468 hasExactSynonym "informed consent form" @default.
- NCIT_C16468 inSubset NCIT_C114548 @default.
- NCIT_C16468 inSubset NCIT_C132298 @default.
- NCIT_C16468 inSubset NCIT_C184334 @default.
- NCIT_C16468 inSubset NCIT_C61410 @default.
- NCIT_C16468 inSubset NCIT_C67497 @default.
- NCIT_C16468 type Class @default.
- NCIT_C16468 isDefinedBy ncit.owl @default.
- NCIT_C16468 label "Consent Form" @default.
- NCIT_C16468 subClassOf NCIT_C16468 @default.
- NCIT_C16468 subClassOf NCIT_C19464 @default.
- NCIT_C16468 subClassOf NCIT_C19498 @default.
- NCIT_C16468 subClassOf NCIT_C20181 @default.
- NCIT_C16468 subClassOf NCIT_C25198 @default.
- NCIT_C16468 subClassOf NCIT_C97331 @default.