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MSZ EN 82304-1:2018

Dokumentumazonosító

167000

Cím

Egészségügyi szoftver. 1. rész: Termékbiztonságra vonatkozó általános követelmények (IEC 82304-1:2016)

Angol cím

Health Software. Part 1: General requirements for product safety (IEC 82304-1:2016)

Alkalmazási terület

1.1 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: a) medical electrical equipment or systems covered by the IEC 60601/IEC 80601 series; b) in vitro diagnostic equipment covered by the IEC 61010 series; or c) implantable devices covered by the ISO 14708 series. NOTE This document also applies to HEALTH SOFTWARE PRODUCTS (e.g. medical apps, health apps) intended to be used in combination with mobile computing platforms. 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. NOTE The term “conformance” is used in ISO/IEC 12207 where the term “compliance” is used in this document.

ICS

35.240.80 Informatikai alkalmazások az egészségügyben

Műszaki Bizottság

A szabvány nyelve

angol

Az érvényesség kezdete

2018-02-01

Forrás

idt EN 82304-1:2017

Előd

Utód

Módosítás

Kiegészítő információk

SZK-közlemények

Kapcsolódó európai jogszabály

98/79/EK AZ EURÓPAI PARLAMENT ÉS A TANÁCS 98/79/EK IRÁNYELVE (1998. október 27.) az in vitro diagnosztikai orvostechnikai eszközökről (VITD); 90/385/EGK A TANÁCS IRÁNYELVE (1990. június 20.) az aktív beültethető orvostechnikai eszközökre vonatkozó tagállami jogszabályok közelítéséről (90/385/EGK) (IMD90); 93/42/EGK A TANÁCS 93/42/EGK IRÁNYELVE (1993. június 14.) az orvostechnikai eszközökről (MDV93)

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