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Medical Devices

Computational modeling and analysis is giving biomedical engineers a competitive advantage by reducing risk, lowering costs, and accelerating innovation.

Improving product reliability and time to market in the medical device industry

Simulation methods for reducing risk and accelerating innovation

By optimizing design, medical device corporations can reduce
time to market and increase product reliability while meeting
budgetary and regulatory requirements.
MSC Software enables the successful adoption of virtual test and simulation methods for medical device manufacturers. Rather than rely on point analysis tools, engineers can now explore a full range of complex simulations when designing medical applications. MSC solutions offer a suite of integrated productivity tools and techniques for managing the entire simulation process while establishing best practices and standards for virtual testing across the enterprise.

Medical device manufacturers face significant regulatory, operational, and business challenges in creating and delivering products to the marketplace. Two business drivers are changing traditional product development: 1. Reduced tolerance among shareholders for product recalls 2. The need to reduce time to market and stay ahead of the competition At the same time, compliance with governmental regulation increases costs and introduces delays. Product development managers and quality assurance personnel must therefore answer the following key questions: 1. How can we optimize the design within a reasonable timeframe? 2. How can we improve product development while still following regulatory processes that maintain safety and reliability? By relying more and more on computational modeling & simulation, medical device manufacturers can achieve rapid verification with virtual models while reducing reliance on the slow, costly process of physical testing. MSC Software provides simulation solutions and best practices for accelerating the process of concept design, performance validation, and regulatory approval across the medical device industry. The Limitations of Physical Testing Adequate physical testing of new medical products is a lengthy and expensive process. At best, it may provide data on failure limits, but does not allow engineers to understand the reasons for each failure. At worst, it can be inconsistent, cost-prohibitive, and incapable of providing any meaningful insight into the interaction between biomedical devices and the human body. Some manufacturers continue to spend millions of dollars on test equipment and thousands of hours on product testing. However, as more and more product development managers embrace the importance of accelerating development and tracing design decisions, simulation has emerged as an ideal means to achieve major improvements in design processes.
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