HL7 Terminology (THO)
7.0.1 - Continuous Process Integration (ci build)
This page is part of the HL7 Terminology (v7.0.1: Release) based on FHIR (HL7® FHIR® Standard) v5.0.0. This is the current published version in its permanent home (it will always be available at this URL). For a full list of available versions, see the Directory of published versions
| Official URL: http://terminology.hl7.org/ValueSet/research-study-party-role | Version: 1.0.0 | |||
| Active as of 2025-11-14 | Maturity Level: 1 | Responsible: Health Level Seven International | Computable Name: ResearchStudyPartyRole | |
| Other Identifiers: OID:2.16.840.1.113883.4.642.3.3075 | ||||
Copyright/Legal: This material derives from the HL7 Terminology (THO). THO is copyright ©1989+ Health Level Seven International and is made available under the CC0 designation. For more licensing information see: https://terminology.hl7.org/license |
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This is a ResearchStudy's party role.
References
This value set is not used here; it may be used elsewhere (e.g. specifications and/or implementations that use this content)
Last updated: 2025-11-14 20:54:02+0000
http://terminology.hl7.org/CodeSystem/research-study-party-role version 📦1.0.0
Expansion performed internally based on codesystem Research Study Party Role v1.0.0 (CodeSystem)
This value set contains 12 concepts
| System | Code | Display (en) | Definition | JSON | XML |
http://terminology.hl7.org/CodeSystem/research-study-party-role | sponsor | Sponsor | Person, company, agency or institution that initiates a clinical investigation and takes responsibility for that investigation but does not conduct the investigation. | ||
http://terminology.hl7.org/CodeSystem/research-study-party-role | lead-sponsor | Lead sponsor | Primary person, company, agency or institution that initiates a clinical investigation and takes responsibility for that investigation but does not conduct the investigation if there is more than one sponsor. | ||
http://terminology.hl7.org/CodeSystem/research-study-party-role | sponsor-investigator | Sponsor-investigator | Entity who both initiates and conducts an investigation. | ||
http://terminology.hl7.org/CodeSystem/research-study-party-role | primary-investigator | Principal investigator | An investigator who is responsible for all aspects of the conduct of a study. | ||
http://terminology.hl7.org/CodeSystem/research-study-party-role | collaborator | Collaborator | An organization or individual, who contributes to a study by providing support to the primary investigator to conduct research. | ||
http://terminology.hl7.org/CodeSystem/research-study-party-role | funding-source | Funding source | An organization that underwrites financial support for the research study. | ||
http://terminology.hl7.org/CodeSystem/research-study-party-role | general-contact | General contact | Information for the person who can answer general questions for a study. | ||
http://terminology.hl7.org/CodeSystem/research-study-party-role | recruitment-contact | Recruitment contact | Information for the person who can answer recruitment questions for a study. | ||
http://terminology.hl7.org/CodeSystem/research-study-party-role | sub-investigator | Sub-investigator | Any individual member of the clinical trial team designated and supervised by the investigator at a trial site to perform critical trial-related procedures and/or to make important trial-related decisions (e.g., associates, residents, research fellows). | ||
http://terminology.hl7.org/CodeSystem/research-study-party-role | study-chair | Study chair | An individual person who both initiates and conducts, alone or with others, a clinical trial and under whose immediate direction the investigational product is administered to, dispensed to, or used by a subject. (Also called study director or study chairperson) | ||
http://terminology.hl7.org/CodeSystem/research-study-party-role | irb | Institutional Review Board | A group of individuals that reviews and monitors research involving human subjects. | ||
http://terminology.hl7.org/CodeSystem/research-study-party-role | data-monitoring | Data Monitoring | An organization or individual who monitors the validity and integrity of collected data while prioritizing participant safety and study integrity. The organization may be called a Data Monitoring Committee (DMC) or Data and Safety Monitoring Board (DSMB). |
Explanation of the columns that may appear on this page:
| Level | A few code lists that FHIR defines are hierarchical - each code is assigned a level. In this scheme, some codes are under other codes, and imply that the code they are under also applies |
| System | The source of the definition of the code (when the value set draws in codes defined elsewhere) |
| Code | The code (used as the code in the resource instance) |
| Display | The display (used in the display element of a Coding). If there is no display, implementers should not simply display the code, but map the concept into their application |
| Definition | An explanation of the meaning of the concept |
| Comments | Additional notes about how to use the code |
History
| Date | Action | Custodian | Author | Comment |
| 2025-11-14 | create | FMG | Joanne Dehnbostel | Move Research Study Party Role Code System and ValueSet from FHIR to THO; up-753 |