CEN ISO/TS 13972:2015

European foreword
Foreword
Introduction
1 Scope
2 Terms and definition
3 Abbreviated terms
4 Definition, purpose, contexts and position
  of Detailed Clinical Models
5 Requirements and Methodology for Detailed
  Clinical Models
Annex A (informative) - Data type profile used for
        the logical model parts for Detailed Clinical
        Models
Annex B (informative) - Example Detailed Clinical Model
        in UML and Table format
Bibliography

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.