SPL Mapping FHIR R5 Implementation Guide, published by HL7 International / Biomedical Research and Regulation. This guide is not an authorized publication; it is the continuous build for version 0.2.1 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/fhir-spl/ and changes regularly. See the Directory of published versions
Page standards status: Trial-use | Maturity Level: 1 |
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"div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p class=\"res-header-id\"><b>Generated Narrative: ValueSet valueset-labelerBusinessOperations</b></p><a name=\"valueset-labelerBusinessOperations\"> </a><a name=\"hcvalueset-labelerBusinessOperations\"> </a><a name=\"valueset-labelerBusinessOperations-en-US\"> </a><ul><li>Include these codes as defined in <a href=\"http://terminology.hl7.org/6.0.2/CodeSystem-v3-nciThesaurus.html\"><code>http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl</code></a><table class=\"none\"><tr><td style=\"white-space:nowrap\"><b>Code</b></td><td><b>Display</b></td></tr><tr><td>C25391</td><td>ANALYSIS</td></tr><tr><td>C101509</td><td>API/FDF ANALYTICAL TESTING</td></tr><tr><td>C82401</td><td>API MANUFACTURE</td></tr><tr><td>C101511</td><td>CLINICAL BIOEQUIVALENCE OR BIOAVAILABILITY STUDY</td></tr><tr><td>C73608</td><td>DISTRIBUTES DRUG PRODUCTS UNDER OWN PRIVATE LABEL</td></tr><tr><td>C101510</td><td>FDF MANUFACTURE</td></tr><tr><td>C112113</td><td>HUMAN DRUG COMPOUNDING OUTSOURCING FACILITY</td></tr><tr><td>C101512</td><td>IN VITRO BIOEQUIVALENCE OR BIOANALYTICAL TESTING</td></tr><tr><td>C84732</td><td>LABEL</td></tr><tr><td>C43360</td><td>MANUFACTURE</td></tr><tr><td>C84635</td><td>MEDICATED ANIMAL FEED MANUFACTURE</td></tr><tr><td>C122061</td><td>OUTSOURCING ANIMAL DRUG COMPOUNDING</td></tr><tr><td>C84731</td><td>PACK</td></tr><tr><td>C84386</td><td>PARTICLE SIZE REDUCTION</td></tr><tr><td>C91403</td><td>POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION</td></tr><tr><td>C73607</td><td>RELABEL</td></tr><tr><td>C73606</td><td>REPACK</td></tr><tr><td>C70827</td><td>SALVAGE</td></tr><tr><td>C175317</td><td>SIP FOREIGN SELLER</td></tr><tr><td>C118412</td><td>THIRD-PARTY LOGISTICS PROVIDER</td></tr><tr><td>C125710</td><td>TRANSFILL</td></tr><tr><td>C118411</td><td>WHOLESALE DRUG DISTRIBUTOR</td></tr></table></li></ul></div>"
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"url" : "http://hl7.org/fhir/us/spl/ValueSet/valueset-labelerBusinessOperations",
"version" : "0.2.1",
"name" : "LabelerBusinessOperations",
"title" : "Labeler Business Operations",
"status" : "active",
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"date" : "2024-10-26T03:36:34+00:00",
"publisher" : "HL7 International / Biomedical Research and Regulation",
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"description" : "The set of business operations that can be specified for a labelling facility.",
"jurisdiction" : [
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"coding" : [
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"code" : "US",
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"system" : "http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl",
"concept" : [
{
"code" : "C25391",
"display" : "ANALYSIS"
},
{
"code" : "C101509",
"display" : "API/FDF ANALYTICAL TESTING"
},
{
"code" : "C82401",
"display" : "API MANUFACTURE"
},
{
"code" : "C101511",
"display" : "CLINICAL BIOEQUIVALENCE OR BIOAVAILABILITY STUDY"
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{
"code" : "C73608",
"display" : "DISTRIBUTES DRUG PRODUCTS UNDER OWN PRIVATE LABEL"
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{
"code" : "C101510",
"display" : "FDF MANUFACTURE"
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{
"code" : "C112113",
"display" : "HUMAN DRUG COMPOUNDING OUTSOURCING FACILITY"
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{
"code" : "C101512",
"display" : "IN VITRO BIOEQUIVALENCE OR BIOANALYTICAL TESTING"
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{
"code" : "C84732",
"display" : "LABEL"
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{
"code" : "C43360",
"display" : "MANUFACTURE"
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{
"code" : "C84635",
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{
"code" : "C122061",
"display" : "OUTSOURCING ANIMAL DRUG COMPOUNDING"
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{
"code" : "C84731",
"display" : "PACK"
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{
"code" : "C84386",
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{
"code" : "C91403",
"display" : "POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION"
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{
"code" : "C73607",
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{
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{
"code" : "C70827",
"display" : "SALVAGE"
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{
"code" : "C175317",
"display" : "SIP FOREIGN SELLER"
},
{
"code" : "C118412",
"display" : "THIRD-PARTY LOGISTICS PROVIDER"
},
{
"code" : "C125710",
"display" : "TRANSFILL"
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{
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