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- NCIT_C142588 IAO_0000115 "The detailed documentation about an individual in a clinical trial that is compiled and managed by the investigator. This includes information on informed consent, medical records and other observations." @default.
- NCIT_C142588 NCIT_NHC0 "C142588" @default.
- NCIT_C142588 NCIT_P106 "Intellectual Product" @default.
- NCIT_C142588 NCIT_P108 "Investigational Subject Case History" @default.
- NCIT_C142588 NCIT_P208 "CL545946" @default.
- NCIT_C142588 NCIT_P322 "CDISC-GLOSS" @default.
- NCIT_C142588 NCIT_P325 "An adequate and accurate record prepared and maintained by an investigator that records all observations and other data pertinent to the investigation of each individual administered the investigational drug (device or other therapy) or employed as a control in the investigation. NOTE: Case histories include the case report forms and supporting data including, for example, signed and dated consent forms and medical records including, for example, progress notes of the physician, the individual's hospital chart(s), and the nurses' notes. The case history for each individual shall document that informed consent was obtained prior to participation in the study. [21 CFR 312.62(b)]" @default.
- NCIT_C142588 normalizedInformationContent "100" @default.
- NCIT_C142588 referenceCount "1" @default.
- NCIT_C142588 hasExactSynonym "Investigational Subject Case History" @default.
- NCIT_C142588 hasExactSynonym "case history" @default.
- NCIT_C142588 inSubset NCIT_C61410 @default.
- NCIT_C142588 inSubset NCIT_C67497 @default.
- NCIT_C142588 type Class @default.
- NCIT_C142588 isDefinedBy ncit.owl @default.
- NCIT_C142588 label "Investigational Subject Case History" @default.
- NCIT_C142588 subClassOf NCIT_C142588 @default.
- NCIT_C142588 subClassOf NCIT_C19498 @default.
- NCIT_C142588 subClassOf NCIT_C20181 @default.
- NCIT_C142588 subClassOf NCIT_C25198 @default.
- NCIT_C142588 subClassOf NCIT_C97331 @default.