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

: 3.2.P.2.2.4 - Summary for Risk of Impurities

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    <div xmlns="http://www.w3.org/1999/xhtml"><p class="res-header-id"><b>Generated Narrative: Composition composition-drug-pq-risk</b></p><a name="composition-drug-pq-risk"> </a><a name="hccomposition-drug-pq-risk"> </a><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"/><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>: <span title="Codes:">Product Note - Summary for Risk of Impurities</span></p><p><b>date</b>: 2023-10-01</p><p><b>author</b>: <a href="Organization-organization-drug-pq-ex1.html">Organization AAA Molybdenum Products, Inc.</a></p><p><b>title</b>: 3.2.P.2.2.4 - Summary for Risk of Impurities</p></div>
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    <text value="Product Note - Summary for Risk of Impurities"/>
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  <date value="2023-10-01"/>
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    <reference value="Organization/organization-drug-pq-ex1"/>
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  <title value="3.2.P.2.2.4 - Summary for Risk of Impurities"/>
  <section>
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      <div xmlns="http://www.w3.org/1999/xhtml"><p>Text for the risk assessment of elemental impurities in the product</p></div>
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