Pharmaceutical Quality (Industry)
1.0.0 - STU1 International flag

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

: Pharmaceutical Report Type Codes - XML Representation

Active as of 2024-05-08

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<CodeSystem xmlns="http://hl7.org/fhir">
  <id value="pharmaceutical-report-type"/>
  <text>
    <status value="generated"/>
    <div xmlns="http://www.w3.org/1999/xhtml"><p>This case-sensitive code system <code>http://terminology.hl7.org/CodeSystem/pharmaceutical-report-type</code> defines the following codes:</p><table class="codes"><tr><td style="white-space:nowrap"><b>Code</b></td></tr><tr><td style="white-space:nowrap">Batch Analysis Report<a name="pharmaceutical-report-type-BatchAnalysisReport"> </a></td></tr><tr><td style="white-space:nowrap">Process Validation Report<a name="pharmaceutical-report-type-ProcessValidationReport"> </a></td></tr><tr><td style="white-space:nowrap">Stability Study Report - 18 months<a name="pharmaceutical-report-type-StabilityStudyReport-18months"> </a></td></tr><tr><td style="white-space:nowrap">Stability Study Report<a name="pharmaceutical-report-type-StabilityStudyReport"> </a></td></tr><tr><td style="white-space:nowrap">Product Compatibility Report<a name="pharmaceutical-report-type-ProductCompatibilityReport"> </a></td></tr><tr><td style="white-space:nowrap">Reference Standard Report<a name="pharmaceutical-report-type-ReferenceStandardReport"> </a></td></tr><tr><td style="white-space:nowrap">Characterization Report<a name="pharmaceutical-report-type-CharacterizationReport"> </a></td></tr><tr><td style="white-space:nowrap">Impurities Report<a name="pharmaceutical-report-type-ImpuritiesReport"> </a></td></tr><tr><td style="white-space:nowrap">Microbiological Attributes Report<a name="pharmaceutical-report-type-MicrobiologicalAttributesReport"> </a></td></tr></table></div>
  </text>
  <extension
             url="http://hl7.org/fhir/StructureDefinition/structuredefinition-wg">
    <valueCode value="brr"/>
  </extension>
  <url
       value="http://terminology.hl7.org/CodeSystem/pharmaceutical-report-type"/>
  <identifier>
    <system value="urn:ietf:rfc:3986"/>
    <value value="urn:oid:2.16.840.1.113883.4.642.40.41.16.27"/>
  </identifier>
  <version value="1.0.0"/>
  <name value="CsPharmReportType"/>
  <title value="Pharmaceutical Report Type Codes"/>
  <status value="active"/>
  <experimental value="false"/>
  <date value="2024-05-08T12:53:57+00:00"/>
  <publisher value="HL7 International / Biomedical Research and Regulation"/>
  <contact>
    <name value="HL7 International - Biomedical Research and Regulation"/>
    <telecom>
      <system value="url"/>
      <value value="http://www.hl7.org/Special/committees/rcrim"/>
    </telecom>
  </contact>
  <description
               value="This code system contains  codes for pharmaceutical report type."/>
  <jurisdiction>
    <coding>
      <system value="http://unstats.un.org/unsd/methods/m49/m49.htm"/>
      <code value="001"/>
      <display value="World"/>
    </coding>
    <text value="World"/>
  </jurisdiction>
  <caseSensitive value="true"/>
  <content value="complete"/>
  <concept>
    <code value="Batch Analysis Report"/>
    <display value="Batch Analysis Report"/>
  </concept>
  <concept>
    <code value="Process Validation Report"/>
    <display value="Process Validation Report"/>
  </concept>
  <concept>
    <code value="Stability Study Report - 18 months"/>
    <display value="Stability Study Report - 18 months"/>
  </concept>
  <concept>
    <code value="Stability Study Report"/>
    <display value="Stability Study Report"/>
  </concept>
  <concept>
    <code value="Product Compatibility Report"/>
    <display value="Product Compatibility Report"/>
  </concept>
  <concept>
    <code value="Reference Standard Report"/>
    <display value="Reference Standard Report"/>
  </concept>
  <concept>
    <code value="Characterization Report"/>
    <display value="Characterization Report"/>
  </concept>
  <concept>
    <code value="Impurities Report"/>
    <display value="Impurities Report"/>
  </concept>
  <concept>
    <code value="Microbiological Attributes Report"/>
    <display value="Microbiological Attributes Report"/>
  </concept>
</CodeSystem>