Pharmaceutical Quality (Industry)
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Pharmaceutical Quality (Industry), published by HL7 International / Biomedical Research and Regulation. This guide is not an authorized publication; it is the continuous build for version 1.0.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/uv-dx-pq/ and changes regularly. See the Directory of published versions

: Composition - Drug - example, formulation - XML Representation

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<Composition xmlns="http://hl7.org/fhir">
  <id value="composition-drug-pq-formulation"/>
  <!--     Based on Accumulus FHIR Product Example - Drug Product  -->
  <meta>
    <profile
             value="http://hl7.org/fhir/uv/pharm-quality/StructureDefinition/Composition-drug-pq"/>
  </meta>
  <text>
    <status value="generated"/>
    <div xmlns="http://www.w3.org/1999/xhtml"><p><b>Generated Narrative: Composition</b><a name="composition-drug-pq-formulation"> </a><a name="hccomposition-drug-pq-formulation"> </a></p><div style="display: inline-block; background-color: #d9e0e7; padding: 6px; margin: 4px; border: 1px solid #8da1b4; border-radius: 5px; line-height: 60%"><p style="margin-bottom: 0px">Resource Composition &quot;composition-drug-pq-formulation&quot; </p><p style="margin-bottom: 0px">Profile: <a href="StructureDefinition-Composition-drug-pq.html">Composition - Drug PQ</a></p></div><p><b>status</b>: final</p><p><b>type</b>: Product Note - Formulation Development <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> ()</span></p><p><b>date</b>: 2023-10-01</p><p><b>author</b>: <a href="Organization-organization-drug-pq-ex1.html">Organization/organization-drug-pq-ex1</a> &quot;AAA Molybdenum Products, Inc.&quot;</p><p><b>title</b>: 3.2.P.2.2.1 - Formulation Development</p></div>
  </text>
  <status value="final"/>
  <type>
    <text value="Product Note - Formulation Development"/>
  </type>
  <subject>🔗 
    <reference
               value="MedicinalProductDefinition/medicinalproductdefinition-drug-product-pq-ex1"/>
  </subject>
  <date value="2023-10-01"/>
  <author>🔗 
    <reference value="Organization/organization-drug-pq-ex1"/>
  </author>
  <title value="3.2.P.2.2.1 - Formulation Development"/>
  <section>
    <title value="3.2.P.2.2.1.1 - Formulation History"/>
    <text>
      <status value="additional"/>
      <div xmlns="http://www.w3.org/1999/xhtml">
                <ul>
                    <li>Drug product description including difference or similarity between the drug product and reference product, if applicable</li>
                    <li>Propose route of administration (include any dilution or reconstitution necessary)</li>
                                <li>Choice of manufacturing process, explain choice if alternative process could have been applicable (e.g. aseptic processing instead of terminal sterilization, direct compression instead of granulation). If different processes were used for different formulation highlight and explain differences, refer at 3.2.P.2.3. If no change in the process occurred refer to 3.3.P.3.3 and avoid duplication data.</li>
                </ul>
                <p>Table 1 - Formulation history for Stelbatolol</p>
                <table>
                    <tr>
                                    <th>Formulation Identifier</th>
                                    <th>Composition</th>
                                    <th>Change</th>
                                    <th>Development phase</th>
                    </tr>
                    <tr>
                                    <td>1233545</td>
                                    <td>Composition 1a</td>
                                    <td>Changes made are listed here</td>
                                    <td>Pre-clinical phase</td>
                    </tr>
                </table>
                            
            </div>
    </text>
  </section>
  <section>
    <title value="3.2.P.2.2.1.2 - Formulation Development Studies"/>
    <text>
      <status value="additional"/>
      <div xmlns="http://www.w3.org/1999/xhtml">
                <p>Summary of the formulation developmental studies conducted are provided in Table 2</p>
                <p>Table 2 - Formulation Development Studies</p>
                <table>
                    <tr>
                                    <th>Study</th>
                                    <th>Formulation identifier </th>
                                    <th>Objective</th>
                                    <th>Quality attribute evaluated</th>
                                    <th>Study design</th>
                                    <th>Study result</th>
                                </tr>
                                <tr>
                                    <td>Study Name</td>
                                    <td>12234a</td>
                                    <td>Short description of the study objective</td>
                                    <td>CQA information</td>
                                    <td>Short description of the design</td>
                                    <td>Reference to the table showing study results</td>
                    </tr>
                </table>
                            
            </div>
    </text>
  </section>
  <section>
    <title
           value="3.2.P.2.2.4 - Summary for Risk Assessment of Elemental Impurities in Drug Product"/>
    <text>
      <status value="additional"/>
      <div xmlns="http://www.w3.org/1999/xhtml">
                <p>Summary of the risk assessment for product...</p>
            </div>
    </text>
  </section>
</Composition>