The SES/Force-4 Team uses proven alternatives to the traditional build-test-modify-repeat model for developing medical devices that can reduce time-to-market by as much as 25%.
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In Silico Design Verification Testing of Medical Devices
Once computational modeling and simulation (CM&S) was officially sanctioned by the FDA, “regulatory grade analysis” has become a rapidly growing trend in medical device development. SES Force-4’s leveraging of computational modeling and simulation based approaches...
