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Narrative

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Source1

{
  "resourceType": "Task",
  "id": "scenario3-04-cta-rfi-response",
  "meta": {
    "versionId": "2",
    "lastUpdated": "2026-10-12T16:00:00+02:00",
    "profile": [
      "http://hl7.org/fhir/uv/apix/StructureDefinition/apix-task"
    ]
  },
  "text": {
    "status": "generated",
    "div": "<!-- snip (see above) -->"
  },
  "identifier": [
    {
      "use": "official",
      "type": {
        "coding": [
          {
            "system": "http://hl7.org/fhir/uv/rwi-pharma/CodeSystem/apix-demo",
            "code": "apixtaskinstance",
            "display": "APIX Task Instance ID"
          }
        ]
      },
      "system": "http://example.org/health-authority/task-id",
      "value": "urn:uuid:d1bba8de-3301-5250-b6aa-6dbc38489f29"
    },
    {
      "use": "official",
      "type": {
        "coding": [
          {
            "system": "http://hl7.org/fhir/uv/rwi-pharma/CodeSystem/apix-demo",
            "code": "apixregulatorprocedureno",
            "display": "APIX Regulator Procedure Number"
          }
        ]
      },
      "system": "http://example.org/health-authority/clinical-trial-number",
      "value": "CT-2026-000789"
    }
  ],
  "basedOn": [
    {
      "reference": "Task/scenario3-01-cta-submission"
    }
  ],
  "groupIdentifier": {
    "use": "official",
    "system": "http://example.org/health-authority/work-flow-group-id",
    "value": "urn:uuid:0a57b9f1-fc39-5bae-a93a-c86bd94484a5"
  },
  "status": "completed",
  "businessStatus": {
    "coding": [
      {
        "system": "http://hl7.org/fhir/uv/rwi-pharma/CodeSystem/apix-business-status",
        "code": "clock-restart",
        "display": "Clock Restart"
      }
    ]
  },
  "intent": "proposal",
  "priority": "routine",
  "code": {
    "coding": [
      {
        "system": "http://hl7.org/fhir/uv/rwi-pharma/CodeSystem/apix-task-code",
        "code": "information-request",
        "display": "List of Questions / Information Request"
      }
    ]
  },
  "requestedPeriod": {
    "start": "2026-10-01T11:00:00+02:00",
    "end": "2026-10-15T23:59:59+02:00"
  },
  "executionPeriod": {
    "start": "2026-10-01T11:05:00+02:00",
    "end": "2026-10-12T16:00:00+02:00"
  },
  "authoredOn": "2026-10-01T11:00:00+02:00",
  "lastModified": "2026-10-12T16:00:00+02:00",
  "requester": {
    "reference": "Organization/org-ema-srm-hmed",
    "display": "Health Authority – Regulatory Review Division"
  },
  "owner": {
    "reference": "Organization/org-synthpharma-ag",
    "display": "SynthPharma AG"
  },
  "input": [
    {
      "type": {
        "coding": [
          {
            "system": "http://hl7.org/fhir/uv/rwi-pharma/CodeSystem/apix-task-input-output-type",
            "code": "request-for-information",
            "display": "Request for Information"
          }
        ]
      },
      "valueReference": {
        "reference": "DocumentReference/docref-cta-rfi",
        "display": "Request for information"
      }
    }
  ],
  "output": [
    {
      "type": {
        "coding": [
          {
            "system": "http://hl7.org/fhir/uv/rwi-pharma/CodeSystem/apix-task-input-output-type",
            "code": "response-to-questions",
            "display": "Response to Questions"
          }
        ]
      },
      "valueReference": {
        "reference": "DocumentReference/docref-cta-rfi-response",
        "display": "Response to request for information"
      }
    }
  ]
}