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API STD 12R1: Installation, Operation, Maintenance, Inspection, and Repair of Tanks in Production Service

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285

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API Technical Report 2583 – Measurement of Produced Water for Custody Transfer

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174

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API Bulletin 592 – Elements of a Fixed Equipment Mechanical Integrity (FE MI) Program

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142

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API SPEC Q1: Addenda 2

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0

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API TR 2583 : Measurement of Produced Water for Custody Transfer

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174

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API TR 2581: Wet Gas Sampling

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189

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API TR 2581 Wet Gas Sampling : Errata 1

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API 510: Pressure Vessel Inspection Code: In-service Inspection, Rating, Repair, and Alteration

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481

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API SPEC 6AV1: Validation of Safety and Shutdown Valves for Sandy Service : Edition 4

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ISO 13972:2022

ISO 13972:2022 Health informatics – Clinical information models – Characteristics, structures and requirements

CDN $351.00

Description

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.

Edition

1

Published Date

2022-02-28

Status

PUBLISHED

Pages

77

Language Detail Icon

English

Format Secure Icon

Secure PDF

Abstract

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.

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