This page is part of the FHIR Specification v6.0.0-ballot1: Release 6 Ballot (1st Draft) (see Ballot Notes). The current version is 5.0.0. For a full list of available versions, see the Directory of published versions
Biomedical Research and Regulation Work Group | Maturity Level: N/A | Standards Status: Informative | Compartments: No 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: RegulatedAuthorization
Resource RegulatedAuthorization "example"
identifier: id: EU/1/11/999/001
region: EU (country#EU)
status: active (authorizationstatus#active)
statusDate: 2015-01-14
validityPeriod: 2014-09-03 --> 2020-05-20
holder: Organization/example
regulator: Organization/example
case
identifier: id: EMEA/H/C/009999/IA/0099/G
type: VariationTypeIA (marketingAuthorizationProcedureType#VariationTypeIA)
date: 2014-09-02 --> 2015-08-21
Applications
Identifier Type Date[x] id: IA38G GroupTypeIAVariationNotification (marketingAuthorizationApplicationType#GroupTypeIAVariationNotification) 2015-08-01 id: IA38F GroupTypeIAVariationNotification (marketingAuthorizationApplicationType#GroupTypeIAVariationNotification) 2014-09-01
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.