Medical devices are typically developed as stand-alone units. Current industrial Verification and Validation (V&V) techniques primarily target stand-alone systems. Moreover, the US Food and Drug Administration's (FDA) regulatory clearance processes are designed to approve such devices that are integrated by a single manufacturer with complete control over all components.
The International Conference on Computing Technology, Information Security and Risk Management (CTISRM2016)
Islamic Azad University, Academic City, Dubai, UAE
March 3-5, 2016 http://sdiwc.net/conferences/ctisrm2016/
