This page is part of the FHIR Specification (v3.5.0: R4 Ballot #2). The current version which supercedes this 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 | Ballot Status: Informative | Compartments: Not linked to any defined compartments |
Raw XML (canonical form + also see XML Format Specification)
Example of medicinalproductauthorization (id = "example")
<?xml version="1.0" encoding="UTF-8"?> <MedicinalProductAuthorization xmlns="http://hl7.org/fhir"> <id value="example"/> <text> <status value="generated"/> <div xmlns="http://www.w3.org/1999/xhtml"><p> <b> Generated Narrative with Details</b> </p> <p> <b> id</b> : example</p> <p> <b> identifier</b> : EU/1/11/999/001</p> <p> <b> country</b> : EU <span> (Details : {http://ema.europa.eu/example/country code 'EU' = 'EU)</span> </p> <p> <b> legalStatusOfSupply</b> : Subjecttomedicalprescription <span> (Details : {http://ema.europa.eu/example/legalstatusofsupply code 'Subjecttomedicalprescription' = 'Subjecttomedicalprescription)</span> </p> <p> <b> status</b> : active <span> (Details : {http://ema.europa.eu/example/authorisationstatus code 'active' = 'active)</span> </p> <p> <b> statusDate</b> : 14/01/2015</p> <p> <b> validityPeriod</b> : 16/08/2015 --> 20/05/2020</p> <p> <b> dataExclusivityPeriod</b> : 15/08/2010 --> 15/08/2020</p> <p> <b> dateOfFirstAuthorization</b> : 15/08/2010</p> <p> <b> internationalBirthDate</b> : 15/08/2010</p> <blockquote> <p> <b> jurisdictionalAuthorization</b> </p> <p> <b> identifier</b> : 123-456-789</p> <p> <b> country</b> : NO <span> (Details : {http://ema.europa.eu/example/countryCode code 'NO' = 'NO)</span> </p> </blockquote> <blockquote> <p> <b> jurisdictionalAuthorization</b> </p> <p> <b> identifier</b> : 123-456-123</p> <p> <b> country</b> : NO <span> (Details : {http://ema.europa.eu/example/countryCode code 'NO' = 'NO)</span> </p> </blockquote> <p> <b> holder</b> : <a> Organization/example</a> </p> <p> <b> regulator</b> : <a> Organization/example</a> </p> <blockquote> <p> <b> procedure</b> </p> <p> <b> identifier</b> : EMEA/H/C/009999/IA/0099/G</p> <p> <b> type</b> : VariationTypeIA <span> (Details : {http://ema.europa.eu/example/marketingAuthorisationProcedureType code 'VariationTypeIA' = 'VariationTypeIA)</span> </p> <p> <b> date</b> : 02/08/2015 --> 21/08/2015</p> <h3> Applications</h3> <table> <tr> <td> -</td> </tr> <tr> <td> *</td> </tr> </table> </blockquote> </div> </text> <identifier> <system value="http://ema.europa.eu/example/marketingAuthorisationNumber"/> <value value="EU/1/11/999/001"/> </identifier> <country> <coding> <system value="http://ema.europa.eu/example/country"/> <code value="EU"/> </coding> </country> <legalStatusOfSupply> <coding> <system value="http://ema.europa.eu/example/legalstatusofsupply"/> <code value="Subjecttomedicalprescription"/> </coding> </legalStatusOfSupply> <status> <coding> <system value="http://ema.europa.eu/example/authorisationstatus"/> <code value="active"/> </coding> </status> <statusDate value="2015-01-14"/> <validityPeriod> <start value="2015-08-16"/> <end value="2020-05-20"/> </validityPeriod> <dataExclusivityPeriod> <start value="2010-08-15"/> <end value="2020-08-15"/> </dataExclusivityPeriod> <dateOfFirstAuthorization value="2010-08-15"/> <internationalBirthDate value="2010-08-15"/> <jurisdictionalAuthorization id="1"> <identifier> <system value="http://ema.europa.eu/example/marketingauthorisationnumber"/> <value value="123-456-789"/> </identifier> <country> <coding> <system value="http://ema.europa.eu/example/countryCode"/> <code value="NO"/> </coding> </country> </jurisdictionalAuthorization> <jurisdictionalAuthorization id="2"> <identifier> <system value="http://ema.europa.eu/example/marketingauthorisationnumber"/> <value value="123-456-123"/> </identifier> <country> <coding> <system value="http://ema.europa.eu/example/countryCode"/> <code value="NO"/> </coding> </country> </jurisdictionalAuthorization> <holder> <reference value="Organization/example"/> </holder> <regulator> <reference value="Organization/example"/> </regulator> <procedure> <identifier> <system value="http://ema.europa.eu/example/procedureidentifier-number"/> <value value="EMEA/H/C/009999/IA/0099/G"/> </identifier> <type> <coding> <system value="http://ema.europa.eu/example/marketingAuthorisationProcedureType"/> <code value="VariationTypeIA"/> </coding> </type> <datePeriod> <start value="2015-08-02"/> <end value="2015-08-21"/> </datePeriod> <application> <identifier> <system value="http://ema.europa.eu/example/applicationidentifier-number"/> <value value="IA38G"/> </identifier> <type> <coding> <system value="http://ema.europa.eu/example/marketingAuthorisationApplicationType"/> <code value="GroupTypeIAVariationNotification"/> </coding> </type> <dateDateTime value="2015-08-01"/> </application> </procedure> </MedicinalProductAuthorization>
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.