FHIR IG Statistics: CodeSystem/100000155531

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{
  "resourceType": "CodeSystem",
  "status": "active",
  "content": "complete",
  "name": "DocumentTypeCs",
  "id": "100000155531",
  "title": "Document Type",
  "description": "Document Type",
  "url": "https://spor.ema.europa.eu/v1/lists/100000155531",
  "concept": [
    {
      "code": "100000155532",
      "display": "Summary of Product Characteristics"
    },
    {
      "code": "100000155533",
      "display": "Annex II"
    },
    {
      "code": "100000155534",
      "display": "Outer Packaging"
    },
    {
      "code": "100000155535",
      "display": "Labelling"
    },
    {
      "code": "100000155536",
      "display": "Immediate Packaging"
    },
    {
      "code": "100000155537",
      "display": "Other Product Information"
    },
    {
      "code": "100000155538",
      "display": "Package Leaflet"
    },
    {
      "code": "100000155539",
      "display": "Combined File of all Documents"
    },
    {
      "code": "100000155540",
      "display": "Mock ups"
    },
    {
      "code": "100000155541",
      "display": "Appendix V"
    },
    {
      "code": "200000017121",
      "display": "Package Leaflet and Labelling"
    },
    {
      "code": "200000027914",
      "display": "Specimens"
    },
    {
      "code": "200000027915",
      "display": "List of all authorised presentations (Annex A)"
    },
    {
      "code": "200000027916",
      "display": "Restrictions posed by Member States (Annex 127a)"
    }
  ],
  "meta": {
    "versionId": "5.0.0",
    "lastUpdated": "2023-08-03T11:35:00.198Z"
  },
  "version": "5.0.0",
  "experimental": false,
  "publisher": "European Medicines Agency",
  "jurisdiction": [
    {
      "text": "European Union"
    }
  ],
  "caseSensitive": true,
  "count": 14
}