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- NCIT_C115477 IAO_0000115 "A legally binding document containing the accession by any/all investigators of a clinical trial that all trial activities will conform fully to all regulations as set forth by the law, or any other supervisory authority." @default.
- NCIT_C115477 NCIT_NHC0 "C115477" @default.
- NCIT_C115477 NCIT_P106 "Intellectual Product" @default.
- NCIT_C115477 NCIT_P108 "Clinical Trial Investigator Regulatory Agreement" @default.
- NCIT_C115477 NCIT_P207 "C3899581" @default.
- NCIT_C115477 NCIT_P322 "CareLex" @default.
- NCIT_C115477 NCIT_P325 "A regulatory statement from the investigator required by certain health authorities. Examples are a Qualified Investigator Undertaking form and Clinical Trial Site Information form required by Health Canada. [Adapted from TMF-RM]" @default.
- NCIT_C115477 normalizedInformationContent "100" @default.
- NCIT_C115477 referenceCount "1" @default.
- NCIT_C115477 hasExactSynonym "Clinical Trial Investigator Regulatory Agreement" @default.
- NCIT_C115477 hasExactSynonym "Investigator Regulatory Agreement" @default.
- NCIT_C115477 hasExactSynonym "Invstgr Reg Agrmnt" @default.
- NCIT_C115477 inSubset NCIT_C114548 @default.
- NCIT_C115477 type Class @default.
- NCIT_C115477 isDefinedBy ncit.owl @default.
- NCIT_C115477 label "Clinical Trial Investigator Regulatory Agreement" @default.
- NCIT_C115477 subClassOf NCIT_C115477 @default.
- NCIT_C115477 subClassOf NCIT_C19498 @default.
- NCIT_C115477 subClassOf NCIT_C20181 @default.
- NCIT_C115477 subClassOf NCIT_C25198 @default.
- NCIT_C115477 subClassOf NCIT_C60777 @default.
- NCIT_C115477 subClassOf NCIT_C97331 @default.