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BS EN ISO 13972:2022 – TC

BS EN ISO 13972:2022 – TC

$280.87

Tracked Changes. Health informatics. Clinical information models. Characteristics, structures and requirements

Published By Publication Date Number of Pages
BSI 2022 242
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PDF Catalog

PDF Pages PDF Title
156 undefined
158 European foreword
Endorsement notice
161 Foreword
162 Introduction
165 1 Scope
2 Normative references
3 Terms, definitions and abbreviated terms
3.1 Terms and definitions
171 3.2 Abbreviated terms
172 4 Health care information models – Concept, purpose, contexts and position
4.1 The Concept of Clinical Information Models
174 4.2 Purpose for Clinical Information Models
175 4.3 Context of Health and Care Information Models
177 4.4 Architectural Considerations for Clinical Information Models
4.4.1 General
4.4.2 CIMs in an architectural view
178 4.4.3 CIMs placed in the Generic Component Model
179 4.4.4 The Interoperability and Integration Reference Architecture in ISO 23903
181 4.4.5 Representation of ReEIF through the ISO Interoperability and Integration Reference Architecture Framework
183 5 Quality Management System for Clinical Information Models
5.1 General
5.2 CIMs quality management system
184 5.3 CIMs Requirements
185 5.4 CIMs acceptance, adoption and use
5.5 Achieving quality CIMs
186 5.6 Governance of CIMs
5.7 Repositories of CIMs
5.8 CIMs Development Processes
187 6 Clinical Information Model content, structure and requirements
6.1 Clinical Information Model content and context
188 6.2 Concept specification of a Clinical Information Model
6.3 Purpose of the Concept
6.4 Patient Population for which the Clinical Information Model is intended
6.5 Evidence Base for the Clinical Information Model topic
189 6.6 Description of the information model and its data elements in CIMs
6.6.1 General requirements for the information model
190 6.6.2 Data elements
192 6.6.3 Data Element Name and Identifier
193 6.6.4 Data Element descriptions
6.6.5 Semantic coding of data elements
194 6.6.6 Datatype
195 6.6.7 Value
196 6.6.8 Value set expression
6.6.9 Relationships in CIMs
197 6.6.10 Localization of CIMs
6.7 Example instances
6.8 Interpretation
198 6.9 Constraints or Limitations for use
199 6.10 Instructions for use of CIMs
200 6.11 Care process / dependence
6.12 Issues
201 6.13 Example of the use of a CIM
6.14 References
6.15 Intellectual property issues around Clinical Information Models
203 7 Metadata for clinical information models
7.1 General
7.2 The metadata elements of the Clinical Information Models
207 8 Version management of clinical information models
208 Annex A (informative) Release and maintenance process example in the Netherlands
209 Annex B (informative) Version management backwards compatibility
210 Annex C (informative) Guidelines and principles for Clinical Information Modelling
217 Annex D (informative) Example mapping a CIM to ADL specification: Glasgow Coma Scale
225 Annex E (informative) Datatype profile used for the logical model parts for Clinical Information Models
226 Annex F (informative) Example Clinical Information Model in UML and Table format
228 Annex G (informative) Example Clinical Information Model transformation in HL7® FHIR®
238 Bibliography

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BS EN ISO 13972:2022 - TC
$280.87