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“ISO 15223:2025 Medical devices – Symbols to be used with information to be supplied by the manufacturer – Part 1: General requirements – Amendment 1: Addition of defined term for authorized representative and modified EC REP symbol to not be country or region specific” has been added to your cart. View cart
ISO 9321:2024
ISO 9321:2024 Health informatics – General requirements of multi-centre medical data collaborative analysis
CDN $173.00
Description
This document outlines the general requirements for conducting a multi-centre medical data collaborative analysis, covering various aspects such as system architecture, data storage, data standardization, collaborative research management and security. The data considered in this standard primarily encompasses electronic health record data for multi-centre collaborative researches, including structured data, medical text data, image data, etc.
This standard is applicable to a wide range of individuals and institutions, including developers, maintainers, management personnel, researchers, and data-owning organizations.
Edition
1
Published Date
2024-06-13
Status
PUBLISHED
Pages
18
Language
English
Format
Secure PDF
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Abstract
This document outlines the general requirements for conducting a multi-centre medical data collaborative analysis, covering various aspects such as system architecture, data storage, data standardization, collaborative research management and security. The data considered in this standard primarily encompasses electronic health record data for multi-centre collaborative researches, including structured data, medical text data, image data, etc.
This standard is applicable to a wide range of individuals and institutions, including developers, maintainers, management personnel, researchers, and data-owning organizations.
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