This 3 hour virtual seminar will help you create an integrated medical device software development process that will meet IEC 62304 and ISO 13485 design control requirements, and generate the documentation needed for software as part of a FDA submission.
3-hr Virtual Seminar: Aligning Medical Device Software Development with EU Requirements for a CE Mark (IEC 62304)
25 February 2014, Palo Alto, United States
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Online Event, 2600 E. Bayshore Road, Palo Alto, 94303, United States
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ComplianceOnline
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