Digital Evidence Generation: Simulation and the Digital Twin for Better Medical Device Design
Register today to learn how digital evidence generation can be used to establish product performance, support the verification process and reduce time to clearance of medical devices.
Digital evidence generation is the process of using simulation (the Digital Twin) to establish product performance—an effort supported by the FDA and regulatory agencies worldwide.
Simulation plays a large role in the development of medical devices, saving development costs by optimizing performance and reliability, reducing benchtop tests and clinical trials, and accelerating the regulatory approval process. Digital evidence generation is the process of using simulation (the digital twin) to establish product performance—an effort supported by FDA and regulatory agencies worldwide.
In this webinar, experts discuss how the digital twin can support the verification process and reduce time to clearance.