This webinar will discuss regulatory requirements for the medical device software development process and how the documentation needed for MDD technical files and for FDA submission can be developed as part of that process.
Managing the Software Development Life Cycle to Produce Regulatory Documentation (for Medical Devices)
22 October 2013, Palo Alto, United States
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ComplianceOnline
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Online Event
Online Event, 2600 E. Bayshore Road, California, Palo Alto, 94303, United States
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