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Resource CodeSystem/FHIR Server from package eu.epi.february2025#1.0.0 (93 ms)

Package eu.epi.february2025
Type CodeSystem
Id Id
FHIR Version R5
Source https://simplifier.net/resolve?scope=eu.epi.february2025@1.0.0&canonical=http://ema.europa.eu/fhir/CodeSystem/300000000002
Url http://ema.europa.eu/fhir/CodeSystem/300000000002
Version 5.0.0
Status active
Name EUepiannexIIcodesystem
Title EU EPI Annex II QRD code values
Experimental False
Description EU EPI Annex II QRD code values
Content complete

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Source

{
  "resourceType" : "CodeSystem",
  "status" : "active",
  "content" : "complete",
  "name" : "EUepiannexIIcodesystem",
  "id" : "300000000002",
  "title" : "EU EPI Annex II QRD code values",
  "description" : "EU EPI Annex II QRD code values",
  "version" : "5.0.0",
  "url" : "http://ema.europa.eu/fhir/CodeSystem/300000000002",
  "concept" : [
    {
      "code" : "000000000000",
      "display" : "Code for custom sub-sections (reserved)"
    },
    {
      "code" : "200000029850",
      "display" : "ANNEX II"
    },
    {
      "code" : "200000029851",
      "display" : "A. <MANUFACTURER(S) OF THE BIOLOGICAL ACTIVE SUBSTANCE(S) AND> MANUFACTURER(S) RESPONSIBLE FOR BATCH RELEASE"
    },
    {
      "code" : "200000029852",
      "display" : "B. CONDITIONS OR RESTRICTIONS REGARDING SUPPLY AND USE"
    },
    {
      "code" : "200000029853",
      "display" : "Official batch release"
    },
    {
      "code" : "200000029854",
      "display" : "C. OTHER CONDITIONS AND REQUIREMENTS OF THE MARKETING AUTHORISATION"
    },
    {
      "code" : "200000029855",
      "display" : "Periodic safety update reports (PSURs)"
    },
    {
      "code" : "200000029856",
      "display" : "D. CONDITIONS OR RESTRICTIONS WITH REGARD TO THE SAFE AND EFFECTIVE USE OF THE MEDICINAL PRODUCT"
    },
    {
      "code" : "200000029857",
      "display" : "Risk management plan (RMP)"
    },
    {
      "code" : "200000029858",
      "display" : "Additional risk minimisation measures"
    },
    {
      "code" : "200000029859",
      "display" : "Obligation to conduct post-authorisation measures"
    },
    {
      "code" : "200000029860",
      "display" : "E. SPECIFIC OBLIGATION TO COMPLETE POST-AUTHORISATION MEASURES FOR <THE CONDITIONAL MARKETING AUTHORISATION> <THE MARKETING AUTHORISATION UNDER EXCEPTIONAL CIRCUMSTANCES"
    }
  ],
  "experimental" : false,
  "publisher" : "European Medicines Agency",
  "jurisdiction" : [
    {
      "text" : "European Union"
    }
  ],
  "caseSensitive" : true,
  "count" : 12,
  "text" : {
  }
}

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