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Medicinalproduct-example.xml

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

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

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Example of medicinalproduct (id = "example")

<MedicinalProduct 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> marketingAuthorization</b> : <a> MedicinalProductAuthorization/example</a> </p> <p> <b> packagedMedicinalProduct</b> : <a> MedicinalProductPackaged/example</a> </p> <p> <b> pharmaceuticalProduct</b> : <a> MedicinalProductPharmaceutical/example</a> </p> <p> <b> clinicalParticulars</b> : <a> MedicinalProductClinicals/example</a> </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 (Details: [not stated] code INV = 'INV', stated as 'null')</p> </blockquote> <blockquote> <p> <b> namePart</b> </p> <p> <b> part</b> : 2.5 mg</p> <p> <b> type</b> : STR (Details: [not stated] code STR = 'STR', stated as 'null')</p> </blockquote> <blockquote> <p> <b> namePart</b> </p> <p> <b> part</b> : film-coated tablets</p> <p> <b> type</b> : FRM (Details: [not stated] code FRM = 'FRM', stated as 'null')</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> OperationType</b> </td> <td> <b> AuthorisationReferenceNumber</b> </td> <td> <b> EffectiveDate</b> </td> <td> <b> Manufacturer</b> </td> <td> <b> Regulator</b> </td> </tr> <tr> <td> *</td> <td> Batchrelease <span> (Details : {http://ema.europa.eu/example/manufacturingOperationType code 'Batchrelease'
               = 'Batchrelease)</span> </td> <td> 1324TZ</td> <td> Mar 15, 2013</td> <td> <a> Organization/example</a> </td> <td> <a> Organization/example</a> </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> 
  <marketingAuthorization> 
    <reference value="MedicinalProductAuthorization/example"/> 
  </marketingAuthorization> 
  <packagedMedicinalProduct> 
    <reference value="MedicinalProductPackaged/example"/> 
  </packagedMedicinalProduct> 
  <pharmaceuticalProduct> 
    <reference value="MedicinalProductPharmaceutical/example"/> 
  </pharmaceuticalProduct> 
  <clinicalParticulars> 
    <reference value="MedicinalProductClinicals/example"/> 
  </clinicalParticulars> 
  <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> 
        <code value="INV"/> 
      </type> 
    </namePart> 
    <namePart> 
      <part value="2.5 mg"/> 
      <type> 
        <code value="STR"/> 
      </type> 
    </namePart> 
    <namePart> 
      <part value="film-coated tablets"/> 
      <type> 
        <code value="FRM"/> 
      </type> 
    </namePart> 
    <countryLanguage> 
      <!--    ISO name: /MedicinalProduct/MedicinalProductName/Country-Language/Country    -->
      <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> 
    <operationType> 
      <coding> 
        <system value="http://ema.europa.eu/example/manufacturingOperationType"/> 
        <code value="Batchrelease"/> 
      </coding> 
    </operationType> 
    <authorisationReferenceNumber> 
      <system value="http://ema.europa.eu/example/manufacturingAuthorisationReferenceNumber"/> 
      <value value="1324TZ"/> 
    </authorisationReferenceNumber> 
    <effectiveDate value="2013-03-15"/> 
    <manufacturer> 
      <reference value="Organization/example"/> 
    </manufacturer> 
    <regulator> 
      <reference value="Organization/example"/> 
    </regulator> 
  </manufacturingBusinessOperation> 
</MedicinalProduct> 

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.