FHIR IG Statistics: CodeSystem/research-study-document-types-code-system

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{
  "resourceType": "CodeSystem",
  "id": "research-study-document-types-code-system",
  "text": {
    "status": "generated",
    "div": "<!-- snip (see above) -->"
  },
  "extension": [
    {
      "url": "http://hl7.org/fhir/StructureDefinition/structuredefinition-fmm",
      "valueInteger": 1
    },
    {
      "url": "http://hl7.org/fhir/StructureDefinition/structuredefinition-wg",
      "valueCode": "cds"
    },
    {
      "url": "http://hl7.org/fhir/StructureDefinition/structuredefinition-standards-status",
      "valueCode": "trial-use"
    }
  ],
  "url": "http://hl7.org/fhir/uv/ebm/CodeSystem/research-study-document-types-code-system",
  "identifier": [
    {
      "system": "urn:ietf:rfc:3986",
      "value": "urn:oid:2.16.840.1.113883.4.642.40.44.16.5"
    }
  ],
  "version": "1.0.0-ballot2",
  "name": "ResearchStudyDocumentTypesCodeSystem",
  "title": "Research Study Document Types Code System",
  "status": "active",
  "experimental": false,
  "date": "2025-07-22T23:04:48+00:00",
  "publisher": "HL7 International / Clinical Decision Support",
  "contact": [
    {
      "name": "HL7 International / Clinical Decision Support",
      "telecom": [
        {
          "system": "url",
          "value": "http://www.hl7.org/Special/committees/dss"
        }
      ]
    }
  ],
  "description": "Codes for use in the DocumentReference.type element when referenced from ResearchStudy.relatesTo.targetReference.",
  "jurisdiction": [
    {
      "coding": [
        {
          "system": "http://unstats.un.org/unsd/methods/m49/m49.htm",
          "code": "001",
          "display": "World"
        }
      ]
    }
  ],
  "caseSensitive": true,
  "content": "complete",
  "count": 19,
  "concept": [
    {
      "code": "adverse-event-monitoring-plan",
      "display": "Adverse event monitoring plan",
      "definition": "The detailed protocol for how unintended and undesired experiences and consequences related to a study will be identified, reported, and managed."
    },
    {
      "code": "ancillary-care-plan",
      "display": "Ancillary care plan",
      "definition": "The detailed protocol for treatment and supportive care activities provided during and after the study."
    },
    {
      "code": "auditing-plan",
      "display": "Auditing plan",
      "definition": "The detailed protocol for how research study integrity will be evaluated, monitored, and managed."
    },
    {
      "code": "confidential-personal-data-management-plan",
      "display": "Confidential personal data management plan",
      "definition": "The detailed protocol for how personally identifiable data from a research study will be shared and preserved, and how such data will be protected from inappropriate sharing."
    },
    {
      "code": "consent-form",
      "display": "Consent form",
      "definition": "The document used to obtain and record consent or assent."
    },
    {
      "code": "consent-plan",
      "display": "Consent plan",
      "definition": "The detailed protocol for how consent or assent will be obtained."
    },
    {
      "code": "data-access-plan",
      "display": "Data access plan",
      "definition": "The detailed protocol for how all of some of the research study dataset will be made available."
    },
    {
      "code": "data-management-plan",
      "display": "Data management plan",
      "definition": "The detailed protocol for how data from a study will be collected, preserved, and shared."
    },
    {
      "code": "dataset",
      "display": "Dataset",
      "definition": "The collection of data generated by the research study."
    },
    {
      "code": "dataset-access",
      "display": "Dataset access",
      "definition": "The information related to how to access the dataset."
    },
    {
      "code": "declaration-of-interests",
      "display": "Declaration of interests",
      "definition": "The statement of conflicts of interest for investigators or anyone involved in decisions regardign study methods and reporting."
    },
    {
      "code": "dissemination-plan",
      "display": "Dissemination plan",
      "definition": "The detailed protocol for how research study results will be reported and advertised."
    },
    {
      "code": "education",
      "display": "Education",
      "definition": "Instructional and orientational information."
    },
    {
      "code": "interim-analysis-plan",
      "display": "Interim analysis plan",
      "definition": "The detailed protocol for how data from a study will be analyzed and reported before the completion of study data collection."
    },
    {
      "code": "irb-approval",
      "display": "Institutional Review Board (IRB) approval",
      "definition": "The document that proposed or establishes Institutional Review Board (IRB) approval."
    },
    {
      "code": "software",
      "display": "Software",
      "definition": "The executable tools used to support the conduct and reporting of the research study."
    },
    {
      "code": "software-access",
      "display": "Software access",
      "definition": "The information related to how to access the research software."
    },
    {
      "code": "specimen-plan",
      "display": "Specimen plan",
      "definition": "The detailed protocol for how specimens collected during the study will be managed."
    },
    {
      "code": "statistical-analysis-plan",
      "display": "Statistical analysis plan",
      "definition": "The detailed protocol for stastical methods and reporting procedures for analyzing the data collected from a study."
    }
  ]
}