Release 5 Preview #2

This page is part of the FHIR Specification (v4.4.0: R5 Preview #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 . Page versions: R5 R4B

Medicinalproductdefinition-example.xml

Biomedical Research and Regulation Work GroupMaturity Level: N/AStandards Status: InformativeCompartments: Not linked to any defined compartments

Raw XML (canonical form + also see XML Format Specification)

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Example of medicinalproductdefinition (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 with Details</b> </p> <p> <b> id</b> : example</p> <p> <b> identifier</b> : {mpid}</p> <p> <b> productClassification</b> : WHOAnatomicalTherapeuticChemicalATCClassificationSystem|B01AF02 <span> (Details : {http://ema.europa.eu/example/WHOAnatomicalTherapeuticChemicalATCClassificationSystem
           code 'WHOAnatomicalTherapeuticChemicalATCClassificationSystem|B01AF02' = 'WHOAnatomicalTherapeuticCh
          emicalATCClassificationSystem|B01AF02)</span> </p> <p> <b> attachedDocument</b> : <a> DocumentReference/example</a> </p> <p> <b> masterFile</b> : <a> DocumentReference/example</a> </p> <blockquote> <p> <b> name</b> </p> <p> <b> productName</b> : Equilidem 2.5 mg film-coated tablets</p> <blockquote> <p> <b> namePart</b> </p> <p> <b> part</b> : Equilidem</p> <p> <b> type</b> : INV <span> (Details : {[not stated] code 'INV' = 'INV)</span> </p> </blockquote> <blockquote> <p> <b> namePart</b> </p> <p> <b> part</b> : 2.5 mg</p> <p> <b> type</b> : STR <span> (Details : {[not stated] code 'STR' = 'STR)</span> </p> </blockquote> <blockquote> <p> <b> namePart</b> </p> <p> <b> part</b> : film-coated tablets</p> <p> <b> type</b> : FRM <span> (Details : {[not stated] code 'FRM' = 'FRM)</span> </p> </blockquote> <h3> CountryLanguages</h3> <table> <tr> <td> -</td> <td> <b> Country</b> </td> <td> <b> Jurisdiction</b> </td> <td> <b> Language</b> </td> </tr> <tr> <td> *</td> <td> EU <span> (Details : {http://ema.europa.eu/example/countryCode code 'EU' = 'EU)</span> </td> <td> EU <span> (Details : {http://ema.europa.eu/example/jurisdictionCode code 'EU' = 'EU)</span> </td> <td> EN <span> (Details : {http://ema.europa.eu/example/languageCode code 'EN' = 'EN)</span> </td> </tr> </table> </blockquote> <h3> ManufacturingBusinessOperations</h3> <table> <tr> <td> -</td> <td> <b> Type</b> </td> <td> <b> EffectiveDate</b> </td> <td> <b> Authorization</b> </td> </tr> <tr> <td> *</td> <td/>  <td> 2013-03-15 --&gt; (ongoing)</td> <td/>  </tr> </table> </div> </text> <identifier> 
    <system value="http://ema.europa.eu/example/MPID"/> 
    <value value="{mpid}"/> 
  </identifier> 
  <productClassification> 
    <coding> 
      <system value="http://ema.europa.eu/example/WHOAnatomicalTherapeuticChemicalATCClassificationSystem"/> 
      <code value="WHOAnatomicalTherapeuticChemicalATCClassificationSystem|B01AF02"/> 
    </coding> 
  </productClassification> 
  <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> 
  <manufacturingBusinessOperation> 
    <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> 
  </manufacturingBusinessOperation> 
</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.