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Description of BS EN 82304-1:2017 20171.1 Purpose This Part of 82304 applies to the safety and security of health software products designed to operate on general computing platforms and intended to be placed on the market without dedicated hardware, and its primary focus is on the requirements for manufacturers. 1.2 Field of application This document covers the entire lifecycle including design, development, validation, installation, maintenance, and disposal of health software products. In each referenced standard, the term “medical device” or “medical device software” is to be substituted by the term “health software” or “health software product”, as appropriate. Where the term “patient” is used, either in this document or in a referenced standard, it refers to the person for whose health benefit the health software is used. IEC 82304-1 does not apply to health software which is intended to become part of a specific hardware designed for health use. Specifically, IEC 82304-1 does not apply to:
1.3 Compliance Compliance with this document is determined by inspection of all documentation required by this document. Assessment of compliance is carried out and documented by the manufacturer. Where the health software product is subject to regulatory requirements, external assessment may take place. Where this document normatively references parts or clauses of other standards focused on safety or security, the manufacturer may use alternative methods to demonstrate compliance with the requirements of this document. These alternative methods may be used if the process results of such alternative methods, including traceability, are demonstrably equivalent and the residual risk remains acceptable.
About BSIBSI Group, also known as the British Standards Institution is the national standards body of the United Kingdom. BSI produces technical standards on a wide range of products and services and also supplies certification and standards-related services to businesses. |
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