With the number of FDA-issued warning letters on the rise, medical device manufacturers are spending increasing amounts of time and money on regulatory compliance.
Not only do medical device manufacturers have to address typical design challenges, such as time to market, innovation, cost reduction, and global competition, they must also address intricate patient safety requirements via strict regulatory guidelines.
With SOLIDWORKS design roles and 3DEXPERIENCE Works Simulation, you can test early and often to cost-effectively innovate devices, while meeting strict standards of quality and performance.