ISO 13972:2022
2022-02
Тезис
This document:
— Specifies clinical information models (CIMs) as health and care concepts that can be used to define and to structure information for various purposes in health care, also enabling information reuse;
— Describes requirements for CIMs content, structure and context and specification of their data elements, data element relationships, meta-data and versioning, and provides guidance and examples;
— Specifies key characteristics of CIMs used in conceptual and logical analysis for use cases such as (reference) architectures, information layers, EHR and PHR systems, interoperability, systems integration in the health domain, and secondary use of data including for public health reporting;
— Defines a Quality Management System (QMS) for a systematic and effective governance, quality management, and measurement of CIMs through their lifecycle of development, testing, distribution, application and maintenance;
— Provides principles for the transformation and application of clinical information models through the wide variation of health information technology.
This document excludes:
— Requirements on the content or application of any particular clinical information model or clinical information modelling methodology;
— Specific applications of clinical information models such as for dynamic modelling of workflow;
— Specifications for modelling entire domains or aggregates of many CIMs such as complete assessment documents or discharge summaries. It does not specify CIMs compositions;
— Specification of how to involve specific clinicians, how to carry out governance including information governance, or how to ensure patient safety.
Общая информация
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Текущий статус: ОпубликованоДата публикации: 2022-02Этап: Опубликование международного стандарта [60.60]
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Версия: 1
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Технический комитет :ISO/TC 215ICS :35.240.80
- RSS обновления
Жизненный цикл
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Ранее
ОтозваноISO/TS 13972:2015
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Сейчас
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00
Предварительная стадия
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10
Стадия, связанная с внесением предложения
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20
Подготовительная стадия
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30
Стадия, связанная с подготовкой проекта комитета
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40
Стадия, связанная с рассмотрением проекта международного стандарта
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50
Стадия, на которой осуществляется принятие стандарта
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60
Стадия, на которой осуществляется публикация
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90
Стадия пересмотра
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95
Стадия, на которой осуществляется отмена стандарта
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00
