{
  "resourceType" : "RegulatedAuthorization",
  "id" : "authorizatione2464a7d3d627b9df9bef5bc3b263fb42",
  "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=\"authorizatione2464a7d3d627b9df9bef5bc3b263fb42\"> </a><a name=\"hcauthorizatione2464a7d3d627b9df9bef5bc3b263fb42\"> </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 &quot;authorizatione2464a7d3d627b9df9bef5bc3b263fb42&quot; </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/1/16/1157/005\u00a0(use:\u00a0OFFICIAL)</p><p><b>subject</b>: <a href=\"PackagedProductDefinition-ppd-5a560e54e674db16fdd59f328eff5f5a.html\">PackagedProductDefinition/ppd-5a560e54e674db16fdd59f328eff5f5a</a> &quot;Suliqua 100 units/ml + 50 micrograms/ml solution for injection in a pre-filled pen 10&quot;</p><p><b>type</b>: Marketing Authorisation <span style=\"background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki\"> (rmswi#220000000061)</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>: 2017-01-11 13:28:17+0000</p><p><b>holder</b>: <a href=\"Organization-mah-16019cea3a857659d2c5a2018c2260df.html\">Organization/mah-16019cea3a857659d2c5a2018c2260df</a> &quot;Sanofi-Aventis Groupe&quot;</p><p><b>regulator</b>: <a href=\"Organization-mra-ff74c5498eb163c2fb470e9fd175a0c1.html\">Organization/mra-ff74c5498eb163c2fb470e9fd175a0c1</a> &quot;European Medicines Agency&quot;</p></div>"
  },
  "identifier" : [{
    "use" : "official",
    "system" : "https://spor.ema.europa.eu/pmswi",
    "value" : "EU/1/16/1157/005"
  }],
  "subject" : [{
    "reference" : "PackagedProductDefinition/ppd-5a560e54e674db16fdd59f328eff5f5a"
  }],
  "type" : {
    "coding" : [{
      "system" : "https://spor.ema.europa.eu/rmswi",
      "code" : "220000000061",
      "display" : "Marketing Authorisation"
    }]
  },
  "status" : {
    "coding" : [{
      "system" : "http://hl7.org/fhir/publication-status",
      "code" : "active",
      "display" : "Active"
    }]
  },
  "statusDate" : "2017-01-11T13:28:17Z",
  "holder" : {
    "reference" : "Organization/mah-16019cea3a857659d2c5a2018c2260df"
  },
  "regulator" : {
    "reference" : "Organization/mra-ff74c5498eb163c2fb470e9fd175a0c1"
  }
}