<p>ISO/TS 13972:2015:</p>
<ul>
<li>Describes requirements and recommended methods against which clinicians can gather, analyse and, specify the clinical context, content, and structure of Detailed Clinical Models.</li>
<li>Defines Detailed Clinical Models (DCMs) in terms of an underlying logical model. They are <b>logical models</b> of clinical concepts and can be used to define and to structure clinical information.</li>
<li>Describes requirements and principles for DCMs, meta-data, versioning, content and context specification, data element specification and data element relationships, and provide guidance and examples.</li>
<li>Specifies DCM governance principles to ensure conceptual integrity of all DCM attributes and logical model accuracy.</li>
<li>Describes DCM development and the methodology principles for use that will support the production of quality DCMs to minimize risk and ensure patient safety.</li>
</ul>
Registration number (WIID)
62416
Scope
<p>ISO/TS 13972:2015:</p>
<ul>
<li>Describes requirements and recommended methods against which clinicians can gather, analyse and, specify the clinical context, content, and structure of Detailed Clinical Models.</li>
<li>Defines Detailed Clinical Models (DCMs) in terms of an underlying logical model. They are <b>logical models</b> of clinical concepts and can be used to define and to structure clinical information.</li>
<li>Describes requirements and principles for DCMs, meta-data, versioning, content and context specification, data element specification and data element relationships, and provide guidance and examples.</li>
<li>Specifies DCM governance principles to ensure conceptual integrity of all DCM attributes and logical model accuracy.</li>
<li>Describes DCM development and the methodology principles for use that will support the production of quality DCMs to minimize risk and ensure patient safety.</li>
</ul>
