Pharmaceutical Quality - Chemistry, Manufacturing and Controls (PQ-CMC) Submissions to FDA, published by HL7 International / Biomedical Research and Regulation. This guide is not an authorized publication; it is the continuous build for version 2.0.0-ballot built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/FHIR-us-pq-cmc-fda/ and changes regularly. See the Directory of published versions
Active as of 2024-12-04 |
{
"resourceType" : "ValueSet",
"id" : "pqcmc-impurity-classification-terminology",
"text" : {
"status" : "generated",
"div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p class=\"res-header-id\"><b>Generated Narrative: ValueSet pqcmc-impurity-classification-terminology</b></p><a name=\"pqcmc-impurity-classification-terminology\"> </a><a name=\"hcpqcmc-impurity-classification-terminology\"> </a><a name=\"pqcmc-impurity-classification-terminology-en-US\"> </a><ul><li>Include these codes as defined in <a href=\"http://terminology.hl7.org/6.1.0/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>C176816</td><td>Degradation Product</td></tr><tr><td>C185190</td><td>Elemental Impurities</td></tr><tr><td>C176815</td><td>Residual Solvent</td></tr><tr><td>C134001</td><td>Inorganic</td></tr><tr><td>C176812</td><td>Process Related/Process</td></tr><tr><td>C185192</td><td>Leachables</td></tr><tr><td>C176813</td><td>Product Related</td></tr><tr><td>C92081</td><td>Microbiological</td></tr></table></li></ul></div>"
},
"extension" : [
{
"url" : "http://hl7.org/fhir/StructureDefinition/structuredefinition-wg",
"valueCode" : "brr"
}
],
"url" : "http://hl7.org/fhir/us/pq-cmc-fda/ValueSet/pqcmc-impurity-classification-terminology",
"identifier" : [
{
"system" : "urn:ietf:rfc:3986",
"value" : "urn:oid:2.16.840.1.113883.4.642.40.36.48.36"
}
],
"version" : "2.0.0-ballot",
"name" : "PqcmcImpurityClassificationTerminology",
"title" : "Impurity Classification Terminology",
"status" : "active",
"experimental" : false,
"date" : "2024-12-04T20:50:29+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"
},
{
"system" : "email",
"value" : "brr@lists.HL7.org"
}
]
}
],
"description" : "Terminology used to qualify the information pertaining to impurity classifications in the framework of the Pharmaceutical Quality/Chemistry, Manufacturing and Controls documents.",
"jurisdiction" : [
{
"coding" : [
{
"system" : "urn:iso:std:iso:3166",
"code" : "US",
"display" : "United States of America"
}
]
}
],
"compose" : {
"include" : [
{
"system" : "http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl",
"concept" : [
{
"code" : "C176816",
"display" : "Degradation Product"
},
{
"code" : "C185190",
"display" : "Elemental Impurities"
},
{
"code" : "C176815",
"display" : "Residual Solvent"
},
{
"code" : "C134001",
"display" : "Inorganic"
},
{
"code" : "C176812",
"display" : "Process Related/Process"
},
{
"code" : "C185192",
"display" : "Leachables"
},
{
"code" : "C176813",
"display" : "Product Related"
},
{
"code" : "C92081",
"display" : "Microbiological"
}
]
}
]
}
}