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-plan-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-plan-type</code> defines the following codes:</p><table class=\"codes\"><tr><td style=\"white-space:nowrap\"><b>Code</b></td><td><b>Display</b></td></tr><tr><td style=\"white-space:nowrap\">analytical-procedure<a name=\"pharmaceutical-plan-type-analytical-procedure\"> </a></td><td>Analytical Procedure</td></tr><tr><td style=\"white-space:nowrap\">manufacturing-process<a name=\"pharmaceutical-plan-type-manufacturing-process\"> </a></td><td>Manufacturing Process</td></tr><tr><td style=\"white-space:nowrap\">process-validation<a name=\"pharmaceutical-plan-type-process-validation\"> </a></td><td>Process Validation</td></tr><tr><td style=\"white-space:nowrap\">container-specification<a name=\"pharmaceutical-plan-type-container-specification\"> </a></td><td>Container Specification</td></tr><tr><td style=\"white-space:nowrap\">product-compatibility<a name=\"pharmaceutical-plan-type-product-compatibility\"> </a></td><td>Product Compatibility</td></tr><tr><td style=\"white-space:nowrap\">elucidation-of-structure<a name=\"pharmaceutical-plan-type-elucidation-of-structure\"> </a></td><td>Elucidation of Structure</td></tr><tr><td style=\"white-space:nowrap\">1244577<a name=\"pharmaceutical-plan-type-1244577\"> </a></td><td>Specification Protocol</td></tr><tr><td style=\"white-space:nowrap\">1244566<a name=\"pharmaceutical-plan-type-1244566\"> </a></td><td>Manufacturing Process</td></tr><tr><td style=\"white-space:nowrap\">1244578<a name=\"pharmaceutical-plan-type-1244578\"> </a></td><td>Reference Standard Analysis</td></tr><tr><td style=\"white-space:nowrap\">1244588<a name=\"pharmaceutical-plan-type-1244588\"> </a></td><td>Stability Study Protocol</td></tr></table></div>"
},
"extension" : [
{
"url" : "http://hl7.org/fhir/StructureDefinition/structuredefinition-wg",
"valueCode" : "brr"
}
],
"url" : "http://terminology.hl7.org/CodeSystem/pharmaceutical-plan-type",
"identifier" : [
{
"system" : "urn:ietf:rfc:3986",
"value" : "urn:oid:2.16.840.1.113883.4.642.40.41.16.26"
}
],
"version" : "1.0.0",
"name" : "CsPharmPlanType",
"title" : "Pharmaceutical Plan 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 plan 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" : "analytical-procedure",
"display" : "Analytical Procedure"
},
{
"code" : "manufacturing-process",
"display" : "Manufacturing Process"
},
{
"code" : "process-validation",
"display" : "Process Validation"
},
{
"code" : "container-specification",
"display" : "Container Specification"
},
{
"code" : "product-compatibility",
"display" : "Product Compatibility"
},
{
"code" : "elucidation-of-structure",
"display" : "Elucidation of Structure"
},
{
"code" : "1244577",
"display" : "Specification Protocol"
},
{
"code" : "1244566",
"display" : "Manufacturing Process"
},
{
"code" : "1244578",
"display" : "Reference Standard Analysis"
},
{
"code" : "1244588",
"display" : "Stability Study Protocol"
}
]
}