Software validation for medical devices and software testing ensure quality compliance and cost-efficiency, adapting to evolving regulatory requirements and complex technologies.

Software is a critical component of any active medical device. No matter if the device is legacy or new, medical software V&V tends to be stringent and rigorous, leading to longer testing cycles. As product technology, ecosystem complexity, and the need to expand markets evolve, software v&v for medical devices is likely to become much more resource intensive.