API for the Exchange of Medicinal Product Information (APIX)
0.1.0 - ci-build
API for the Exchange of Medicinal Product Information (APIX), published by Gravitate Health Project. This guide is not an authorized publication; it is the continuous build for version 0.1.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/APIX---API-Exchange-for-Medicinal-Products/ and changes regularly. See the Directory of published versions
{
"resourceType" : "Task",
"id" : "scenario1-07-final-decision",
"meta" : {
"versionId" : "3",
"lastUpdated" : "2025-04-20T09:00:00+01:00",
"profile" : [
🔗 "http://hl7.org/fhir/uv/apix/StructureDefinition/apix-task"
]
},
"text" : {
"status" : "generated",
"div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\">Final Decision: Approval for Type IB Variation</div>"
},
"contained" : [
{
"resourceType" : "Organization",
"id" : "org-synthpharma-ag",
"name" : "SynthPharma AG",
"contact" : [
{
"name" : [
{
"text" : "Dr. John Doe, Head of Regulatory Affairs"
}
],
"telecom" : [
{
"system" : "email",
"value" : "john.doe@synthpharma.example",
"use" : "work"
}
]
}
]
},
{
"resourceType" : "Organization",
"id" : "org-ema-srm-hmed",
"name" : "European Medicines Agency – Human Medicines Evaluation Division",
"contact" : [
{
"name" : [
{
"text" : "Scientific and Regulatory Management"
}
],
"telecom" : [
{
"system" : "email",
"value" : "srm@ema.example.eu",
"use" : "work"
}
]
}
]
},
{
"resourceType" : "DocumentReference",
"id" : "docref-approval-letter",
"meta" : {
"versionId" : "1",
"lastUpdated" : "2025-04-20T09:00:00+01:00",
"profile" : [
🔗 "http://hl7.org/fhir/uv/apix/StructureDefinition/apix-documentreference"
]
},
"status" : "current",
"type" : {
"coding" : [
{
"system" : "http://hl7.org/fhir/uv/apix/CodeSystem/ctd-section",
"code" : "1.0",
"display" : "Cover Letter"
}
]
},
"date" : "2025-04-20T09:00:00+01:00",
"content" : [
{
"attachment" : {
"contentType" : "application/pdf",
"data" : "VGhpcyBpcyBhIHBsYWNlaG9sZGVyIGRvY3VtZW50IGZvciB2YWxpZGF0aW9uIHB1cnBvc2VzLgo=",
"title" : "approval-letter.pdf",
"creation" : "2025-04-20T09:00:00+01:00"
}
}
]
},
{
"resourceType" : "DocumentReference",
"id" : "docref-assessment-report",
"meta" : {
"versionId" : "1",
"lastUpdated" : "2025-04-20T09:00:00+01:00",
"profile" : [
🔗 "http://hl7.org/fhir/uv/apix/StructureDefinition/apix-documentreference"
]
},
"status" : "current",
"type" : {
"coding" : [
{
"system" : "http://hl7.org/fhir/uv/apix/CodeSystem/ctd-section",
"code" : "1.0",
"display" : "Cover Letter"
}
]
},
"date" : "2025-04-20T09:00:00+01:00",
"content" : [
{
"attachment" : {
"contentType" : "application/pdf",
"data" : "VGhpcyBpcyBhIHBsYWNlaG9sZGVyIGRvY3VtZW50IGZvciB2YWxpZGF0aW9uIHB1cnBvc2VzLgo=",
"title" : "final-assessment-report.pdf",
"creation" : "2025-04-20T09:00:00+01:00"
}
}
]
}
],
"identifier" : [
{
"type" : {
"coding" : [
{
"system" : "http://hl7.org/fhir/uv/apix/CodeSystem/apix-identifier-type",
"code" : "task-instance-uuid",
"display" : "Task Instance UUID"
}
]
},
"system" : "urn:ietf:rfc:3986",
"value" : "urn:uuid:999e7d2a-8b1c-4d9f-9a2e-1f6c9d8e7b3d"
}
],
"groupIdentifier" : {
"use" : "official",
"type" : {
"coding" : [
{
"system" : "http://hl7.org/fhir/uv/apix/CodeSystem/apix-identifier-type",
"code" : "submission-group-uuid",
"display" : "Submission Group UUID"
}
]
},
"system" : "urn:ietf:rfc:3986",
"value" : "urn:uuid:workflow-group-id-12345"
},
"partOf" : [
{
🔗 "reference" : "Task/scenario1-01-initial-submission",
"display" : "Initial Submission Task"
}
],
"status" : "completed",
"businessStatus" : {
"coding" : [
{
"system" : "http://hl7.org/fhir/uv/apix/CodeSystem/apix-business-status",
"code" : "approved",
"display" : "Approved"
}
]
},
"intent" : "proposal",
"priority" : "routine",
"code" : {
"coding" : [
{
"system" : "http://hl7.org/fhir/uv/apix/CodeSystem/apix-task-code",
"code" : "approval",
"display" : "Approval Letter / Positive Decision"
}
]
},
"for" : {
"reference" : "MedicinalProductDefinition/example-ma",
"display" : "WonderDrug 50mg Tablets"
},
"authoredOn" : "2025-04-20T09:00:00+01:00",
"lastModified" : "2025-04-20T09:00:00+01:00",
"requester" : {
"reference" : "#org-ema-srm-hmed",
"display" : "European Medicines Agency"
},
"requestedPerformer" : [
{
"reference" : {
"reference" : "#org-synthpharma-ag",
"display" : "SynthPharma AG"
}
}
],
"output" : [
{
"type" : {
"coding" : [
{
"system" : "http://hl7.org/fhir/uv/apix/CodeSystem/apix-task-output-type",
"code" : "regulatory-document"
}
]
},
"valueReference" : {
"reference" : "#docref-approval-letter",
"display" : "Approval Letter"
}
},
{
"type" : {
"coding" : [
{
"system" : "http://hl7.org/fhir/uv/apix/CodeSystem/apix-task-output-type",
"code" : "regulatory-document"
}
]
},
"valueReference" : {
"reference" : "#docref-assessment-report",
"display" : "Final Assessment Report"
}
}
]
}