This page is part of the FHIR Specification (v4.6.0: R5 Draft Ballot). 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 |
Raw XML (canonical form + also see XML Format Specification)
Basic Example of a drug authorization for Equilidem (id = "basic-drug-auth")
<?xml version="1.0" encoding="UTF-8"?> <RegulatedAuthorization xmlns="http://hl7.org/fhir"> <id value="basic-drug-auth"/> <text> <status value="generated"/> <div xmlns="http://www.w3.org/1999/xhtml"><p> <b> Generated Narrative</b> </p> <p> <b> subject</b> : <a> MedicinalProductDefinition/equilidem</a> </p> <p> <b> type</b> : <span> Regulatory Drug Marketing Approval</span> </p> <p> <b> status</b> : <span> active</span> </p> <p> <b> statusDate</b> : 2016-01-01</p> <p> <b> holder</b> : <a> EquiliDrugCo Holdings Inc.</a> </p> <p> <b> regulator</b> : <a> FDA</a> </p> </div> </text> <subject> <reference value="MedicinalProductDefinition/equilidem"/> </subject> <type> <text value="Regulatory Drug Marketing Approval"/> </type> <status> <coding> <code value="active"/> </coding> </status> <statusDate value="2016-01-01"/> <holder> <reference value="Organization/EqlidrugCo"/> <display value="EquiliDrugCo Holdings Inc."/> </holder> <regulator> <reference value="Organization/FDA"/> <display value="FDA"/> </regulator> </RegulatedAuthorization>
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.