This page is part of the Pharmaceutical Quality (Industry) (v1.0.0: STU1) based on FHIR (HL7® FHIR® Standard) v5.0.0. This is the current published version in its permanent home (it will always be available at this URL). For a full list of available versions, see the Directory of published versions
Active as of 2024-05-08 |
<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="2024-05-08T13:23:45+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>