Gravitate Health FHIR Implementation Guide, 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-eu/gravitate-health and changes regularly. See the Directory of published versions
{
"resourceType" : "RegulatedAuthorization",
"id" : "authorizatione3e5e78d4e002ed9e15b925cd546e20b0",
"meta" : {
"profile" : [
🔗 "http://hl7.org/fhir/uv/emedicinal-product-info/StructureDefinition/RegulatedAuthorization-uv-epi"
]
},
"text" : {
"status" : "generated",
"div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p><b>Generated Narrative: RegulatedAuthorization</b><a name=\"authorizatione3e5e78d4e002ed9e15b925cd546e20b0\"> </a><a name=\"hcauthorizatione3e5e78d4e002ed9e15b925cd546e20b0\"> </a></p><div style=\"display: inline-block; background-color: #d9e0e7; padding: 6px; margin: 4px; border: 1px solid #8da1b4; border-radius: 5px; line-height: 60%\"><p style=\"margin-bottom: 0px\">Resource RegulatedAuthorization "authorizatione3e5e78d4e002ed9e15b925cd546e20b0" </p><p style=\"margin-bottom: 0px\">Profile: <a href=\"https://build.fhir.org/ig/HL7/emedicinal-product-info//StructureDefinition-RegulatedAuthorization-uv-epi.html\">RegulatedAuthorization (ePI)</a></p></div><p><b>identifier</b>: <code>https://spor.ema.europa.eu/pmswi</code>/EU/1/13/853/001\u00a0(use:\u00a0OFFICIAL)</p><p><b>subject</b>: <a href=\"MedicinalProductDefinition-mpbe76bdf784deea6950583b234f789db2.html\">MedicinalProductDefinition/mpbe76bdf784deea6950583b234f789db2</a></p><p><b>type</b>: Marketing Authorisation <span style=\"background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki\"> (rmswi#100000072062)</span></p><p><b>status</b>: Active <span style=\"background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki\"> (<a href=\"http://hl7.org/fhir/R5/codesystem-publication-status.html\">PublicationStatus</a>#active)</span></p><p><b>statusDate</b>: 2018-06-21</p><p><b>holder</b>: <a href=\"Organization-mah-3c850a69e5187931f2198c5e63f933fe.html\">Organization/mah-3c850a69e5187931f2198c5e63f933fe</a> "Celltrion Healthcare Hungary Kft."</p><p><b>regulator</b>: <a href=\"Organization-mra-e3da03c458d6c0f3c5f1c39a2c6a1084.html\">Organization/mra-e3da03c458d6c0f3c5f1c39a2c6a1084</a> "European Medicines Agency"</p></div>"
},
"identifier" : [
{
"use" : "official",
"system" : "https://spor.ema.europa.eu/pmswi",
"value" : "EU/1/13/853/001"
}
],
"subject" : [
{
🔗 "reference" : "MedicinalProductDefinition/mpbe76bdf784deea6950583b234f789db2"
}
],
"type" : {
"coding" : [
{
"system" : "https://spor.ema.europa.eu/rmswi",
"code" : "100000072062",
"display" : "Marketing Authorisation"
}
]
},
"status" : {
"coding" : [
{
"system" : "http://hl7.org/fhir/publication-status",
"code" : "active",
"display" : "Active"
}
]
},
"statusDate" : "2018-06-21",
"holder" : {
🔗 "reference" : "Organization/mah-3c850a69e5187931f2198c5e63f933fe"
},
"regulator" : {
🔗 "reference" : "Organization/mra-e3da03c458d6c0f3c5f1c39a2c6a1084"
}
}