This page is part of the HL7 Terminology (v1.0.0: Release) based on FHIR R4. The current version which supercedes this version is 5.2.0. For a full list of available versions, see the Directory of published versions

RoleClassClinicalResearchSponsor - XML Representation

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Raw xml

Source view

<ValueSet xmlns="http://hl7.org/fhir">
  <id value="v3-RoleClassClinicalResearchSponsor"/>
  <language value="en"/>
  <text>
    <status value="generated"/>
    <div xmlns="http://www.w3.org/1999/xhtml" xml:lang="en" lang="en"><h2>RoleClassClinicalResearchSponsor</h2><div><p>A role played by an entity, usually an organization, that is the sponsor of a clinical research trial or study. The sponsor commissions the study, bears the expenses, is responsible for satisfying all legal requirements concerning subject safety and privacy, and is generally responsible for collection, storage and analysis of the data generated during the trial. No scoper is necessary, as a clinical research sponsor undertakes the role on its own authority and declaration. Clinical research sponsors are usually educational or other research organizations, government agencies or biopharmaceutical companies.</p>
</div><ul><li>Include codes from <a href="CodeSystem-v3-RoleClass.html"><code>http://terminology.hl7.org/CodeSystem/v3-RoleClass</code></a> where concept  is-a  <a href="CodeSystem-v3-RoleClass.html#v3-RoleClass-CRSPNSR">CRSPNSR</a></li></ul></div>
  </text>
  <url
       value="http://terminology.hl7.org/ValueSet/v3-RoleClassClinicalResearchSponsor"/>
  <identifier>
    <system value="urn:ietf:rfc:3986"/>
    <value value="urn:oid:2.16.840.1.113883.1.11.20126"/>
  </identifier>
  <version value="2.0.0"/>
  <name value="RoleClassClinicalResearchSponsor"/>
  <title value="RoleClassClinicalResearchSponsor"/>
  <status value="active"/>
  <date value="2014-03-26T00:00:00-04:00"/>
  <description
               value="A role played by an entity, usually an organization, that is the sponsor of a clinical research trial or study. The sponsor commissions the study, bears the expenses, is responsible for satisfying all legal requirements concerning subject safety and privacy, and is generally responsible for collection, storage and analysis of the data generated during the trial. No scoper is necessary, as a clinical research sponsor undertakes the role on its own authority and declaration. Clinical research sponsors are usually educational or other research organizations, government agencies or biopharmaceutical companies."/>
  <immutable value="true"/>
  <compose>
    <include>
      <system value="http://terminology.hl7.org/CodeSystem/v3-RoleClass"/>
      <filter>
        <property value="concept"/>
        <op value="is-a"/>
        <value value="CRSPNSR"/>
      </filter>
    </include>
  </compose>
</ValueSet>