Projekta Nr.ISO/TS 13972:2015
Nosaukums<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>
Reģistrācijas numurs (WIID)62416
Darbības sfēra<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>
StatussAtcelts
ICS grupa35.240.80