Human factors engineering plays a large role in the design of medical devices. The goal is to minimize use errors and risks so physicians can use the devices safely and effectively to treat patients. The FDA acknowledges the need for simulation as digital evidence. FDA regulations for medical devices help the industry standardize verification and validation (V&V) of simulation and modeling to provide better outcomes.
By generating digital evidence in V&V testing, medical device manufacturers can ensure a safe and efficacious product. Learn more about how using digital evidence can achieve design excellence.
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