How Amendments to the Medical Device Directive Affect the Development of Medical Device Software
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[1] Paul L Jones,et al. Risk management in the design of medical device software systems. , 2002, Biomedical instrumentation & technology.
[2] Martin Höst,et al. A Snapshot of the State of Practice in Software Development for Medical Devices , 2007, ESEM 2007.
[3] Tilo Messer,et al. Siemens process assessment and improvement approaches: experiences and benefits , 1998, Proceedings. The Twenty-Second Annual International Computer Software and Applications Conference (Compsac '98) (Cat. No.98CB 36241).
[4] En Iso,et al. DECLARATION OF CONFORMITY TO COUNCIL DIRECTIVE 93/42/EEC (INCLUDING DIRECTIVE 2007/47/EEC) CONCERNING MEDICAL DEVICES , 2010 .
[5] Fergal Mc Caffery,et al. The Need for a Software Process Improvement Model for the Medical Device Industry , 2007 .
[6] Marvin V. Zelkowitz,et al. Lessons learned from 25 years of process improvement: the rise and fall of the NASA software engineering laboratory , 2002, Proceedings of the 24th International Conference on Software Engineering. ICSE 2002.
[7] Fergal McCaffery,et al. Medi SPICE: An Overview , 2009 .
[8] Michael Daskalantonakis,et al. A Practical View of Software Measurement and Implementation Experiences Within Motorola , 1992, IEEE Trans. Software Eng..
[9] Tore Dybå,et al. An empirical investigation of the key factors for success in software process improvement , 2005, IEEE Transactions on Software Engineering.