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 |
{
"resourceType" : "ValueSet",
"id" : "valueset-gdufaFacilityBusinessOperations",
"text" : {
"status" : "generated",
"div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p class=\"res-header-id\"><b>Generated Narrative: ValueSet valueset-gdufaFacilityBusinessOperations</b></p><a name=\"valueset-gdufaFacilityBusinessOperations\"> </a><a name=\"hcvalueset-gdufaFacilityBusinessOperations\"> </a><a name=\"valueset-gdufaFacilityBusinessOperations-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>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>C101510</td><td>FDF MANUFACTURE</td></tr><tr><td>C101512</td><td>IN VITRO BIOEQUIVALENCE OR BIOANALYTICAL TESTING</td></tr><tr><td>C84731</td><td>PACK</td></tr><tr><td>C91403</td><td>POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION</td></tr><tr><td>C73606</td><td>REPACK</td></tr></table></li></ul></div>"
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"_valueInteger" : {
"extension" : [
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"url" : "http://hl7.org/fhir/StructureDefinition/structuredefinition-conformance-derivedFrom",
"valueCanonical" : "http://hl7.org/fhir/us/spl/ImplementationGuide/hl7.fhir.us.spl"
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"url" : "http://hl7.org/fhir/us/spl/ValueSet/valueset-gdufaFacilityBusinessOperations",
"version" : "0.2.1",
"name" : "GDUFAFacilityBusinessOperations",
"title" : "GDUFA Facility 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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"name" : "HL7 International / Biomedical Research and Regulation",
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"value" : "http://www.hl7.org/Special/committees/rcrim"
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],
"description" : "The set of business operations that can be specified for a GDUFA facility.",
"jurisdiction" : [
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"coding" : [
{
"system" : "urn:iso:std:iso:3166",
"code" : "US",
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"concept" : [
{
"code" : "C101509",
"display" : "API/FDF ANALYTICAL TESTING"
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{
"code" : "C82401",
"display" : "API MANUFACTURE"
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{
"code" : "C101511",
"display" : "CLINICAL BIOEQUIVALENCE OR BIOAVAILABILITY STUDY"
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{
"code" : "C101510",
"display" : "FDF MANUFACTURE"
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{
"code" : "C101512",
"display" : "IN VITRO BIOEQUIVALENCE OR BIOANALYTICAL TESTING"
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{
"code" : "C84731",
"display" : "PACK"
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{
"code" : "C91403",
"display" : "POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION"
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{
"code" : "C73606",
"display" : "REPACK"
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