Terminology Service < Semantic Lookup Platform

All terms in NCIT

Label	Id	Description
Document Identifier	NCIT_C93399	[The unique identification of a document in a specified context.]
Government Funding	NCIT_C93390	[Fiscal support from governmental organizations.]
Funding Mechanism	NCIT_C20020	[The type of award an agency makes to support a program and within which it incorporates the terms and conditions for expending the funds and performing the work.]
Biologic Entity Group	NCIT_C93391	[A collection of biologic entities.]
Defined Criterion Group	NCIT_C93392	[A collection of conditions joined together via composition (ANDed) and/or optionality (ORed) to form a logical expression upon which the execution of an activity is based or upon which the cessation of a repeated activity is based, where components of the group may include other activities, observation results and/or other criterion groups, and where both the criterion group and it's components are defined as part of the global library.]
Defined Subject Activity Group	NCIT_C93393	[A collection of activities from a global library that would be performed on a common subject at approximately the same time.]
Common Sub-Domain	NCIT_C93383	[The Common sub-domain represents the semantics that are common to all (or most) of the other sub-domains, for example, it includes semantics for such things as people, organizations, places and materials.]
Protocol Representation Sub-Domain	NCIT_C93384	[The Protocol Representation sub-domain is intended for those involved in the planning and design of a research protocol. The majority of business requirements have come from those involved in clinical trial protocols. It focuses on the characteristics of a study and the definition and association of activities within the protocols, including "arms" and "epochs". It also includes the definitions of the roles that participate in those activities.]
Regulatory Sub-Domain	NCIT_C93385	[The Regulatory sub-domain is intended for those involved in the creation and review of submissions to regulatory authorities. The majority of business requirements come from the regulated product submission (RPS) message specification. It focuses on the documentation required for a product submission to the Food and Drug Administration (FDA).]
Study Conduct Sub-Domain	NCIT_C93386	[The Study Conduct sub-domain is intended for those involved in the execution of a research study. The majority of business requirements have come from those involved in clinical trials. It focuses on the activities of conducting the study as well as the results from those activities.]
Associated Biologic Entity	NCIT_C93387	[An individual biologic entity connected/linked to a subject.]
Entity	NCIT_C51070	[An independently existing thing (living or nonliving).]
Experimental Unit	NCIT_C93388	[A physical entity which is the primary unit of interest in a specific research objective. In an interventional study, the experimental unit is assigned to an intervention. The experimental unit is also the unit of primary statistical analysis. Commonly the individual study subject (animal, person or product) is the experimental unit. Different experimental units must be capable of receiving different experimental interventions.]
Randomization Book Entry	NCIT_C93389	[An item/element of a randomization book that can be used to assign a subject to a planned arm or portion of an arm in a study.]
Entry	NCIT_C43381	[An item inserted in a written or electronic record.]
Report Version Document	NCIT_C93380	[A document characterized by information or other content which is tailored to the context of a given situation and audience.]
Study Protocol Document	NCIT_C93381	[A representation of the study protocol (that persists over time) in document form.]
Adverse Event Sub-Domain	NCIT_C93382	[The Adverse Event sub-domain is intended for those involved in safety related activities; such as detection, evaluation, follow-up and reporting. This includes safety issues involving people or products. It also includes activities during or after a research protocol.]
Defined Procedure	NCIT_C93372	[An activity defined at a global library level that is an action whose immediate and primary intention is the alteration of the physical condition of the study subject or experimental unit.]
Defined Specimen Collection	NCIT_C93373	[An activity defined at a global library level that is an action of gathering samples that may be used for subsequent analysis.]