BS EN 62304 deals with medical device software. The amendment adds requirements for legacy software which will help manufacturers demonstrate compliance with the relevant European Directives.
BS EN 62304 on medical device software is relevant to manufacturers of:
BS EN 62304 on medical device software applies to the development and maintenance of medical device software when the software is itself a medical device or when software is embedded or an integral part of the final medical device.
BS EN 62304:2006+A1:2015 adds requirements to deal with legacy software, where the software design is prior to the existence of the current version.
BS EN 62304:2006+A1:2015 will help manufacturers show compliance with the standard in order to meet European Directives. Software safety classification changes needed for this amendment include clarification of requirements and updating of the software safety classification to include a risk-based approach.
EN 60335-2-26:2003/A1:2008
EN 62304:2006/A1:2015
IEC 62304:2006/AMD1:2015