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- NCIT_C16741 IAO_0000115 "A specially constituted independent review body comprised of medical, scientific and non-scientific members established and designated by an entity to ensure the protection of the rights, safety and well-being of human subjects recruited to participate in biomedical or behavioral research according to the requirements outlined in Title 38, part 16 (same as Title 45, part 46 and Title 21, part 56) of the U.S. Code of Federal Regulations. IRB responsibility include but not limited to the reviewing, approving, and providing continuing review of trial protocol and amendments and of the methods and material(s) to be used in obtaining and documenting informed consent of the trial. Other equivalent committees with the same or similar functions are also considered to be IRBs." @default.
- NCIT_C16741 NCIT_NHC0 "C16741" @default.
- NCIT_C16741 NCIT_P106 "Health Care Related Organization" @default.
- NCIT_C16741 NCIT_P108 "Institutional Review Board" @default.
- NCIT_C16741 NCIT_P207 "C0086911" @default.
- NCIT_C16741 NCIT_P322 "CDISC" @default.
- NCIT_C16741 NCIT_P322 "CDISC-GLOSS" @default.
- NCIT_C16741 NCIT_P325 "A group of scientists, doctors, clergy, and consumers that reviews and approves the action plan for every clinical trial. There is an Institutional Review Board at every health care facility that does clinical research. Institutional Review Boards are designed to protect the people who take part in a clinical trial. Institutional Review Boards check to see that the trial is well designed, legal, ethical, does not involve unneccesary risks, and includes safeguards for patients." @default.
- NCIT_C16741 NCIT_P325 "An independent body constituted of medical, scientific, and non-scientific members, whose responsibility is to ensure the protection of the rights, safety and well-being of human subjects involved in a study by, among other things, reviewing, approving, and providing continuing review of study protocol and amendments and of the methods and material to be used in obtaining and documenting informed consent of the study subjects. (ICH E6 R2)" @default.
- NCIT_C16741 NCIT_P325 "An independent body constituted of medical, scientific, and non-scientific members, whose responsibility it is to ensure the protection of the rights, safety, and well-being of human subjects involved in a study by, among other things, reviewing, approving, and providing continuing review of study protocol and of the methods and material to be used in obtaining and documenting informed consent of the study subjects. [ICH E6 1.31]" @default.
- NCIT_C16741 NCIT_P366 "Institutional_Review_Board" @default.
- NCIT_C16741 normalizedInformationContent "100" @default.
- NCIT_C16741 referenceCount "1" @default.
- NCIT_C16741 hasExactSynonym "IRB" @default.
- NCIT_C16741 hasExactSynonym "Institutional Review Board" @default.
- NCIT_C16741 hasExactSynonym "committee for the protection of human subjects" @default.
- NCIT_C16741 hasExactSynonym "independent ethics committee" @default.
- NCIT_C16741 hasExactSynonym "independent review board" @default.
- NCIT_C16741 hasExactSynonym "institutional review board (IRB)" @default.
- NCIT_C16741 inSubset NCIT_C132298 @default.
- NCIT_C16741 inSubset NCIT_C165642 @default.
- NCIT_C16741 inSubset NCIT_C61410 @default.
- NCIT_C16741 inSubset NCIT_C67497 @default.
- NCIT_C16741 type Class @default.
- NCIT_C16741 isDefinedBy ncit.owl @default.
- NCIT_C16741 label "Institutional Review Board" @default.
- NCIT_C16741 subClassOf NCIT_C16741 @default.
- NCIT_C16741 subClassOf NCIT_C17005 @default.
- NCIT_C16741 subClassOf NCIT_C19711 @default.
- NCIT_C16741 subClassOf NCIT_C199143 @default.
- NCIT_C16741 subClassOf NCIT_C20181 @default.
- NCIT_C16741 subClassOf NCIT_C43359 @default.