This paper discusses some best practices for repeatable and exhaustive verification in the Simulink environment. It describes how early verification and validation (V&V) in Model-Based Design can ...
DUBLIN--(BUSINESS WIRE)--The "Understanding FDA Design Verification and Validation Requirements for Medical Devices" webinar has been added to ResearchAndMarkets.com's offering. This webinar will help ...
Medical device companies that identify quality problems early on can prevent product development costs from spiraling out of control, while also laying the groundwork for design verification and ...
Computational models and simulations have had an important role in engineering analysis since as far back as the 1960s. It is widely recognized that the use of modeling and simulation tools can make ...
When it comes to verification and validation, medical device companies need to ensure that what they're doing actually makes sense. Known colloquially as "V&V," for many it feels like you're on the ...
If chip design had a face, it would have a wrinkle or two, an especially deep one caused by the increasingly complex challenge of hardware and software verification. Until recently, these two elements ...
Validation ensures that a part will operate correctly in end-user applications. Design validation is the task of testing a part or a system adequately to ensure that all parts or systems manufactured ...
Why hardware-assisted verification systems are vital to designing next-gen hardware. The differences between hardware emulation and FPGA-based prototyping systems. How the demands of data-center CPUs ...
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