Résumé
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.
Informations générales
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État actuel: AnnuléeDate de publication: 2015-10Stade: Annulation de la Norme internationale [95.99]
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Edition: 1
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Comité technique :ISO/TC 215ICS :35.240.80
- RSS mises à jour
Cycle de vie
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Actuellement
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Révisée par
PubliéeISO 13972:2022