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IEC
IEC TR 80002-3:2014

IEC TR 80002-3:2014

Withdrawn

Withdrawn

A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.

Medical device software - Part 3: Process reference model of medical device software life cycle processes (IEC 62304)

Available format(s)

Hardcopy , PDF , PDF 3 Users , PDF 5 Users , PDF 9 Users

Withdrawn date

03-11-2023

Language(s)

English

Published date

04-06-2014

Publisher

International Electrotechnical Committee

FOREWORD
INTRODUCTION
1 Scope
2 Normative references
3 Terms and definitions
4 Medical device software life cycle processes
Annex A (informative) - Development of this
        technical report
Annex B (informative) - Mapping between IEC 62304:2006
        and ISO/IEC 12207:2008
Bibliography

IEC TR 80002-3:2014 which is a technical report (TR), provides the description of software life cycle processes for medical devices. The medical device software life cycle processes are derived from IEC 62304:2006, with corresponding safety classes. They have been aligned with the software development life cycle processes of ISO/IEC 12207:2008 and are presented herein in full compliance with ISO/IEC 24774:2010. The content of these three standards provides the foundation of this TR. This TR does not:
- address areas already covered by existing related standards, e.g. the international standards that relate to the four standards used to build this TR (see Bibliography);
- FDA guidance documents; or
- software development tools. This TR describes the process reference model for medical device software development and is limited in scope to the life cycle processes described in IEC 62304:2006. The process names correspond to those of IEC 62304:2006. The mappings provided in Annex B are essential for the alignment between IEC 62304:2006 (which is based on ISO/IEC 12207:1995) and ISO/IEC 12207:2008, developed to address the detailed normative relationship between the two standards. This technical report is not intended to be used as the basis of regulatory inspection or certification assessment activities.

DevelopmentNote
Stability date: 2017. (06/2014)
DocumentType
Technical Report
Pages
28
PublisherName
International Electrotechnical Committee
Status
Withdrawn

Standards Relationship
AAMI/IEC TIR80002-3:2016 Identical
NEN NPR IEC/TR 80002-3 : 2014 Identical
PD IEC/TR 80002-3:2014 Identical

VDI 5702 Blatt 1:2017-04 Medical device software - Medical SPICE Process assessment model

ISO/IEC 14764:2006 Software Engineering Software Life Cycle Processes Maintenance
ISO 13485:2016 Medical devices Quality management systems Requirements for regulatory purposes
ISO/IEC 15288:2008 Systems and software engineering System life cycle processes
IEC 62304:2006+AMD1:2015 CSV Medical device software - Software life cycle processes
ISO/IEC 12207:2008 Systems and software engineering Software life cycle processes
ISO 14971:2007 Medical devices Application of risk management to medical devices

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Hardcopy - English
PDF - English
PDF 3 Users - English
PDF 5 Users - English
PDF 9 Users - English
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