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)
General example (id = "example")
<?xml version="1.0" encoding="UTF-8"?> <MedicinalProductDefinition xmlns="http://hl7.org/fhir"> <id value="example"/> <text> <status value="generated"/> <div xmlns="http://www.w3.org/1999/xhtml"> <p> <b> Generated Narrative</b> </p> <p> <b> Id</b> : example</p> <p> <b> Identifier</b> : {mpid}</p> <p> <b> Classification</b> : <span title="Codes: {http://ema.europa.eu/example/WHOAnatomicalTherapeuticChemicalATCClassificationSystem B01AF02}">ATC: B01AF02</span> </p> <p> <b> Attached Document</b> : (SmPC)</p> <p> <b> Master File</b> : (Pharmacovigilence Master File)</p> <p> <b> Product Name</b> : Equilidem 2.5 mg film-coated tablets</p> <blockquote> <p> <b> Name Part</b> </p> <p> <b> part</b> :Equilidem</p> <p> <b> type</b> : <span title="Codes: ">Invented</span> </p> </blockquote> <blockquote> <p> <b> Name Part</b> </p> <p> <b> part</b> :2.5 mg</p> <p> <b> type</b> : <span title="Codes: ">Strength</span> </p> </blockquote> <blockquote> <p> <b> Name Part</b> </p> <p> <b> part</b> :film-coated tablets</p> <p> <b> type</b> : <span title="Codes: ">Form</span> </p> <p> <b> Country & Languages</b> </p> <table class="grid"> <tr> <td> -</td> <td> <b> Country</b> </td> <td> <b> Jurisdiction</b> </td> <td> <b> Language</b> </td> </tr> <tr> <td> *</td> <td> <span title="Codes: {http://ema.europa.eu/example/countryCode EU}">EU</span> </td> <td> <span title="Codes: {http://ema.europa.eu/example/jurisdictionCode EU}">EU</span> </td> <td> <span title="Codes: {http://ema.europa.eu/example/languageCode EN}">EN</span> </td> </tr> </table> </blockquote> <p> <b> Manufacturing & Business Operations</b> </p> <table class="grid"> <tr> <td> -</td> <td> <b> Type</b> </td> <td> <b> EffectiveDate</b> </td> <td> <b> Authorization</b> </td> </tr> <tr> <td> *</td> <td> Batch Release</td> <td> 2013-03-15 --> (ongoing)</td> <td> <span> 1324TZ</span> </td> </tr> </table> </div> </text> <identifier> <system value="http://ema.europa.eu/example/MPID"/> <value value="{mpid}"/> </identifier> <classification> <coding> <system value="http://ema.europa.eu/example/WHOAnatomicalTherapeuticChemicalATCClassificationSystem"/> <code value="B01AF02"/> </coding> </classification> <attachedDocument> <reference value="DocumentReference/example"/> </attachedDocument> <masterFile> <reference value="DocumentReference/example"/> </masterFile> <name> <productName value="Equilidem 2.5 mg film-coated tablets"/> <namePart> <part value="Equilidem"/> <type> <coding> <code value="INV"/> </coding> </type> </namePart> <namePart> <part value="2.5 mg"/> <type> <coding> <code value="STR"/> </coding> </type> </namePart> <namePart> <part value="film-coated tablets"/> <type> <coding> <code value="FRM"/> </coding> </type> </namePart> <countryLanguage> <country> <coding> <system value="http://ema.europa.eu/example/countryCode"/> <code value="EU"/> </coding> </country> <jurisdiction> <coding> <system value="http://ema.europa.eu/example/jurisdictionCode"/> <code value="EU"/> </coding> </jurisdiction> <language> <coding> <system value="http://ema.europa.eu/example/languageCode"/> <code value="EN"/> </coding> </language> </countryLanguage> </name> <operation> <type> <concept> <coding> <system value="http://ema.europa.eu/example/manufacturingOperationType"/> <code value="Batchrelease"/> </coding> </concept> </type> <effectiveDate> <start value="2013-03-15"/> </effectiveDate> <authorization> <identifier> <system value="http://ema.europa.eu/example/manufacturingAuthorisationReferenceNumber"/> <value value="1324TZ"/> </identifier> </authorization> </operation> </MedicinalProductDefinition>
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.