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- NCIT_C16735 IAO_0000115 "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." @default.
- NCIT_C16735 NCIT_A32 NCIT_C177639 @default.
- NCIT_C16735 NCIT_NHC0 "C16735" @default.
- NCIT_C16735 NCIT_P106 "Health Care Activity" @default.
- NCIT_C16735 NCIT_P107 "Informed Consent" @default.
- NCIT_C16735 NCIT_P108 "Informed Consent" @default.
- NCIT_C16735 NCIT_P207 "C0021430" @default.
- NCIT_C16735 NCIT_P322 "CDISC" @default.
- NCIT_C16735 NCIT_P322 "CDISC-GLOSS" @default.
- NCIT_C16735 NCIT_P322 "CTRP" @default.
- NCIT_C16735 NCIT_P322 "GDC" @default.
- NCIT_C16735 NCIT_P325 "A process in which a person is given important facts about a medical procedure or treatment, a clinical trial, or genetic testing before deciding whether or not to participate. It also includes informing the patient when there is new information that may affect his or her decision to continue. Informed consent includes information about the possible risks, benefits, and limits of the procedure, treatment, trial, or genetic testing." @default.
- NCIT_C16735 NCIT_P325 "An ongoing process that provides the subject with explanations that will help in making educated decisions about whether to begin or continue participating in a trial. informed consent is an ongoing, interactive process rather than a one-time information session. NOTE: Under 21 CFR 50.20, no informed consent form may include any "language through which the subject or the representative is made to waive or appear to waive any of the subject's legal rights, or releases or appears to release the investigator, the sponsor, the institution, or its agents from liability for negligence." In some cases, when the prospective subject is unable to provide legal consent, permission to participate may be obtained from a legally-authorized representative. See also consent form." @default.
- NCIT_C16735 NCIT_P325 "Consent given by a subject, or in the case of an individual that can only give assent, by a parent or legal guardian, for the participation in a clinical study only after having achieved an understanding of both the relevant medical facts and the relevant risks involved." @default.
- NCIT_C16735 NCIT_P366 "Informed_Consent" @default.
- NCIT_C16735 NCIT_P375 "Informed Consent" @default.
- NCIT_C16735 normalizedInformationContent "100" @default.
- NCIT_C16735 referenceCount "1" @default.
- NCIT_C16735 hasExactSynonym "Formal Consent" @default.
- NCIT_C16735 hasExactSynonym "INFORMED CONSENT OBTAINED" @default.
- NCIT_C16735 hasExactSynonym "Informed Consent" @default.
- NCIT_C16735 hasExactSynonym "informed consent" @default.
- NCIT_C16735 inSubset NCIT_C114118 @default.
- NCIT_C16735 inSubset NCIT_C116977 @default.
- NCIT_C16735 inSubset NCIT_C118169 @default.
- NCIT_C16735 inSubset NCIT_C132298 @default.
- NCIT_C16735 inSubset NCIT_C132310 @default.
- NCIT_C16735 inSubset NCIT_C157711 @default.
- NCIT_C16735 inSubset NCIT_C177537 @default.
- NCIT_C16735 inSubset NCIT_C61410 @default.
- NCIT_C16735 inSubset NCIT_C66830 @default.
- NCIT_C16735 inSubset NCIT_C67497 @default.
- NCIT_C16735 type Class @default.
- NCIT_C16735 isDefinedBy ncit.owl @default.
- NCIT_C16735 label "Informed Consent" @default.
- NCIT_C16735 subClassOf NCIT_C16326 @default.
- NCIT_C16735 subClassOf NCIT_C16735 @default.
- NCIT_C16735 subClassOf NCIT_C19683 @default.
- NCIT_C16735 subClassOf NCIT_C43431 @default.