This course will introduce all necessary steps to design, implement and test critical medical device software in a regulatory compliant environment. Software risk management has to be embedded into the bigger scope of overall risk management. Therefore this course will additionally address the system level risk management and the resulting interfaces to software.
2-day In-person Seminar on Medical Device Software Risk Management and Assurance Case at Los Angeles, CA
22 - 23 June 2014, Los Angeles, CA, United States
Introduction
Venue
WILL BE ANNOUNCED SOON
WILL BE ANNOUNCED SOON, Los Angeles, CA, Los Angeles, CA, 90012, United States
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Organised by
GlobalCompliancePanel
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