Electronic Medicinal Product Information (ePI) FHIR Implementation Guide
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This page is part of the Electronic Medicinal Product Information (ePI) FHIR Implementation Guide (v1.0.0-ballot: STU1 Ballot 1) based on FHIR v5.0.0-ballot. . For a full list of available versions, see the Directory of published versions

: Regulated Authorization for cava 75 mg tablets - JSON Representation

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{
  "resourceType" : "RegulatedAuthorization",
  "id" : "297e405a-b6f9-4273-bc01-ae031efe47f8",
  "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=\"297e405a-b6f9-4273-bc01-ae031efe47f8\"> </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;297e405a-b6f9-4273-bc01-ae031efe47f8&quot; </p><p style=\"margin-bottom: 0px\">Profile: <a href=\"StructureDefinition-RegulatedAuthorization-uv-epi.html\">RegulatedAuthorization (ePI)</a></p></div><p><b>identifier</b>: id: EU/1/96/007/035 (use: OFFICIAL)</p><p><b>subject</b>: <a href=\"MedicinalProductDefinition-800a51a2-d81d-49a4-a4eb-f2417d301837.html\">MedicinalProductDefinition/800a51a2-d81d-49a4-a4eb-f2417d301837</a></p><p><b>type</b>: Marketing Authorisation <span style=\"background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki\"> (rmswi#100000072062)</span></p><p><b>region</b>: Denmark <span style=\"background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki\"> (<a href=\"http://terminology.hl7.org/5.0.0/CodeSystem-ISO3166Part1.html\">ISO 3166-1 Codes for the representation of names of countries and their subdivisions — Part 1: Country code</a>#DK)</span></p><p><b>status</b>: Active <span style=\"background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki\"> (<a href=\"http://build.fhir.org/codesystem-publication-status.html\">PublicationStatus</a>#active)</span></p><p><b>statusDate</b>: 2015-02-07 13:28:17+0000</p><p><b>holder</b>: <a href=\"Organization-d71bf884-90eb-47f9-81b7-fa81ecec7e75.html\">Organization/d71bf884-90eb-47f9-81b7-fa81ecec7e75</a> &quot;Acme Inc&quot;</p></div>"
  },
  "identifier" : [
    {
      "use" : "official",
      "system" : "https://spor.ema.europa.eu/pmswi",
      "value" : "EU/1/96/007/035"
    }
  ],
  "subject" : [
    {
      "reference" : "MedicinalProductDefinition/800a51a2-d81d-49a4-a4eb-f2417d301837"
    }
  ],
  "type" : {
    "coding" : [
      {
        "system" : "https://spor.ema.europa.eu/rmswi",
        "code" : "100000072062"
      }
    ],
    "text" : "Marketing Authorisation"
  },
  "region" : [
    {
      "coding" : [
        {
          "system" : "urn:iso:std:iso:3166",
          "code" : "DK"
        }
      ],
      "text" : "Denmark"
    }
  ],
  "status" : {
    "coding" : [
      {
        "system" : "http://hl7.org/fhir/publication-status",
        "code" : "active"
      }
    ],
    "text" : "Active"
  },
  "statusDate" : "2015-02-07T13:28:17Z",
  "holder" : {
    "reference" : "Organization/d71bf884-90eb-47f9-81b7-fa81ecec7e75"
  }
}