ISO/TS 13972:2015:
Describes requirements and recommended methods against which clinicians can gather, analyse and, specify the clinical context, content, and structure of Detailed Clinical Models.
Defines Detailed Clinical Models (DCMs) in terms of an underlying logical model. They are logical models of clinical concepts and can be used to define and to structure clinical information.
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.
Specifies DCM governance principles to ensure conceptual integrity of all DCM attributes and logical model accuracy.
Describes DCM development and the methodology principles for use that will support the production of quality DCMs to minimize risk and ensure patient safety.
CSA Group
Done
Description
ISO/TS 13972:2015:
Describes requirements and recommended methods against which clinicians can gather, analyse and, specify the clinical context, content, and structure of Detailed Clinical Models.
Defines Detailed Clinical Models (DCMs) in terms of an underlying logical model. They are logical models of clinical concepts and can be used to define and to structure clinical information.
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.
Specifies DCM governance principles to ensure conceptual integrity of all DCM attributes and logical model accuracy.
Describes DCM development and the methodology principles for use that will support the production of quality DCMs to minimize risk and ensure patient safety.
Health informatics - Detailed clinical models, characteristics and processes
ISO/TS 13972:2015
Health informatics - Detailed clinical models, characteristics and processes
ISO/TS 13972:2015
ISO/TS 13972:2015:
Describes requirements and recommended methods against which clinicians can gather, analyse and, specify the clinical context, content, and structure of Detailed Clinical Models.
Defines Detailed Clinical Models (DCMs) in terms of an underlying logical model. They are logical models of clinical concepts and can be used to define and to structure clinical information.
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.
Specifies DCM governance principles to ensure conceptual integrity of all DCM attributes and logical model accuracy.
Describes DCM development and the methodology principles for use that will support the production of quality DCMs to minimize risk and ensure patient safety.
ISO/TS 13972:2015:
Describes requirements and recommended methods against which clinicians can gather, analyse and, specify the clinical context, content, and structure of Detailed Clinical Models.
Defines Detailed Clinical Models (DCMs) in terms of an underlying logical model. They are logical models of clinical concepts and can be used to define and to structure clinical information.
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.
Specifies DCM governance principles to ensure conceptual integrity of all DCM attributes and logical model accuracy.
Describes DCM development and the methodology principles for use that will support the production of quality DCMs to minimize risk and ensure patient safety.
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Technical Specifications
CSA Group
Product Category
Standards and Technical Documents
Product Number
ISO/TS 13972:2015
Product Name
Health informatics - Detailed clinical models, characteristics and processes
