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. For a full list of available versions, see the Directory of published versions
Active as of 2024-05-08 |
{
"resourceType" : "CodeSystem",
"id" : "pharmaceutical-report-type",
"text" : {
"status" : "generated",
"div" : "<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>"
},
"extension" : [
{
"url" : "http://hl7.org/fhir/StructureDefinition/structuredefinition-wg",
"valueCode" : "brr"
}
],
"url" : "http://terminology.hl7.org/CodeSystem/pharmaceutical-report-type",
"identifier" : [
{
"system" : "urn:ietf:rfc:3986",
"value" : "urn:oid:2.16.840.1.113883.4.642.40.41.16.27"
}
],
"version" : "1.0.0",
"name" : "CsPharmReportType",
"title" : "Pharmaceutical Report Type Codes",
"status" : "active",
"experimental" : false,
"date" : "2024-05-08T13:55:35+00:00",
"publisher" : "HL7 International / Biomedical Research and Regulation",
"contact" : [
{
"name" : "HL7 International - Biomedical Research and Regulation",
"telecom" : [
{
"system" : "url",
"value" : "http://www.hl7.org/Special/committees/rcrim"
}
]
}
],
"description" : "This code system contains codes for pharmaceutical report type.",
"jurisdiction" : [
{
"coding" : [
{
"system" : "http://unstats.un.org/unsd/methods/m49/m49.htm",
"code" : "001",
"display" : "World"
}
],
"text" : "World"
}
],
"caseSensitive" : true,
"content" : "complete",
"concept" : [
{
"code" : "Batch Analysis Report",
"display" : "Batch Analysis Report"
},
{
"code" : "Process Validation Report",
"display" : "Process Validation Report"
},
{
"code" : "Stability Study Report - 18 months",
"display" : "Stability Study Report - 18 months"
},
{
"code" : "Stability Study Report",
"display" : "Stability Study Report"
},
{
"code" : "Product Compatibility Report",
"display" : "Product Compatibility Report"
},
{
"code" : "Reference Standard Report",
"display" : "Reference Standard Report"
},
{
"code" : "Characterization Report",
"display" : "Characterization Report"
},
{
"code" : "Impurities Report",
"display" : "Impurities Report"
},
{
"code" : "Microbiological Attributes Report",
"display" : "Microbiological Attributes Report"
}
]
}