HL7 Terminology (THO)
6.1.0 - Continuous Process Integration (ci build) International flag

HL7 Terminology (THO), published by HL7 International - Vocabulary Work Group. This guide is not an authorized publication; it is the continuous build for version 6.1.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/UTG/ and changes regularly. See the Directory of published versions

: Medical Dictionary for Regulatory Activities - XML Representation

Active as of 2023-06-14

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<CodeSystem xmlns="http://hl7.org/fhir">
  <id value="mdr"/>
  <text>
    <status value="generated"/>
    <div xmlns="http://www.w3.org/1999/xhtml"><p class="res-header-id"><b>Generated Narrative: CodeSystem mdr</b></p><a name="mdr"> </a><a name="hcmdr"> </a><a name="mdr-en-US"> </a><p>This case-sensitive code system <code>https://www.meddra.org</code> defines codes, but no codes are represented here</p></div>
  </text>
  <url value="https://www.meddra.org"/>
  <identifier>
    <system value="urn:ietf:rfc:3986"/>
    <value value="urn:oid:2.16.840.1.113883.6.163"/>
  </identifier>
  <version value="3.0.0"/>
  <name value="MedDRA"/>
  <title value="Medical Dictionary for Regulatory Activities"/>
  <status value="active"/>
  <experimental value="false"/>
  <date value="2023-06-14T00:00:00-04:00"/>
  <publisher
             value="MedDRA Maintenance and Support Services Organization (MedDRA MSSO); Mr. Patrick Revelle; MSSO Director"/>
  <contact>
    <name
          value="International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH)"/>
    <telecom>
      <system value="url"/>
      <value value="https://www.ich.org/page/contact"/>
    </telecom>
  </contact>
  <description
               value="MedDRA is a multilingual standardised international medical terminology which can be used for regulatory communication and evaluation of data pertaining to medicinal products for human use.  MedDRA is designed for use in the registration, documentation and safety monitoring of medicinal products through all phases of the development cycle (i.e., from clinical trials to post-marketing surveillance).#13;

MedDRA is structured as a five level hierarchy. System Organ Classes (SOCs) are the broadest terms (e.g., Cardiac disorders, Investigations). The lowest level of the terminology is the Lowest Level Term (LLT) level."/>
  <copyright
             value="Please see [https://www.meddra.org/legal-mentions](https://www.meddra.org/legal-mentions). For information about special licensing, see [https://www.meddra.org/subscription/special-licences](https://www.meddra.org/subscription/special-licences)"/>
  <caseSensitive value="true"/>
  <content value="not-present"/>
</CodeSystem>