This page is part of the FHIR Specification (v4.2.0: R5 Preview #1). The current version which supercedes this version is 5.0.0. For a full list of available versions, see the Directory of published versions . Page versions: R5 R4B
Biomedical Research and Regulation Work Group | Maturity Level: N/A | Standards Status: Informative | Compartments: Not linked to any defined compartments |
This is the narrative for the resource. See also the XML, JSON or Turtle format. This example conforms to the profile RegulatedAuthorization.
Generated Narrative with Details
id: example
identifier: EU/1/11/999/001
region: EU (Details : {http://ema.europa.eu/example/country code 'EU' = 'EU)
status: active (Details : {http://ema.europa.eu/example/authorisationstatus code 'active' = 'active)
statusDate: 2015-01-14
validityPeriod: 2015-08-16 --> 2020-05-20
jurisdictionalAuthorization: RegulatedAuthorization/Jurusdictional1
holder: Organization/example
regulator: Organization/example
case
identifier: EMEA/H/C/009999/IA/0099/G
type: VariationTypeIA (Details : {http://ema.europa.eu/example/marketingAuthorisationProcedureType code 'VariationTypeIA' = 'VariationTypeIA)
date: 2015-08-02 --> 2015-08-21
Applications
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Usage note: every effort has been made to ensure that the examples are correct and useful, but they are not a normative part of the specification.