Medical Device Simulation
With patient welfare hanging in the balance, disruptive innovation is a permanent concern and product failure is not an option in healthcare. Applying engineering simulation throughout development can make all the difference in bringing new treatments to patients while meeting safety standards and product deadlines.
When you build reliability into the design process, it improves compliance with tightening FDA regulations — and saves lives. Since clinical testing can’t address every possible situation, medical device companies adopt engineering simulation (in silico testing) to systematically identify and resolve worst-case scenarios.
- Case Studies
- White Papers
- Hearts Content - Article - ANSYS Advantage - V10 I3
- Wired into Health - Article - ANSYS Advantage - V10 I2
- Cardiovascular Engineering - Article - ANSYS Advantage - V7 I2
- In Your Blood - Article - ANSYS Advantage - V8 I1
- Change of Heart - Article - ANSYS Advantage - V8 I2
- Heart to Heart - Article - ANSYS Advantage - V7 I3
- Cut to the Bone - Article - ANSYS Advantage - V5 I2
- A New System for Surgery - Article - ANSYS Advantage - V6 I1
- Engineering Solutions for Infection Control - Article - ANSYS Advantage - V1 I2
- Taming the Cost of Respiratory Drug Development - Article - ANSYS Advantage - V4 I2
- 10 Compelling Reasons to Upgrade to ANSYS 17.0 for Healthcare Applications - Webinar
- Vertical Medical Applications: Bringing Simulation to Clinicians - Webinar
- What are Healthcare Thought Leaders Foreseeing for 2016 - Webinar
- Nonlinear Modeling for Health Care Applications - Webinar
- ANSYS Convergence Webinar Series 2013: Business of Simulation - Exponent - Webinar
- Streamline Mixing Analysis and Enable Quality by Design Using ANSYS Workbench - Webinar
- Predicting MR Compliance of Implanted Devices - Webinar
- Assessment of Turbulent Blood Flow Using CFD - Webinar
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Implantable cardiovascular devices — stents, coils, heart valves and pacemakers — are complex as a result of exacting product and regulatory (FDA) specifications. The study of hemodynamics is critical to cardiac device engineering, which can benefit greatly from engineering simulation and advanced fluid–structure interaction modeling.
Engineering simulation is a proven way to optimize diagnostic equipment. The trend is toward smaller, smarter, more portable and more accurate devices.
"Smart" medical equipment and supplies incorporate multifunctional electronic and microelectronic capabilities, which add complexity to the product engineering process.
As life expectancy rises, orthopedic researchers are extending the life of joint implants and developing innovative replacement therapies for aging hips, knees, shoulders and spines. Successful companies invest heavily in engineering simulation to develop the best possible design while ensuring implantable product reliability.
Globalization addresses the lack of engineering resources in non-industrialized countries. It also enables the healthcare industry to customize global concepts (device, product or process) to meet local needs.
Affordable & Profitable Medicine
Affordable treatment and product profitability are not at odds: Successful healthcare companies streamline the long, costly testing and approval process yet still engineer innovative medical and pharmaceutical solutions.
Ensuring Extreme Reliability
Regulatory approval includes subjecting products, procedures and services to the extreme conditions they will encounter during use — over a large patient population. ANSYS technology helps minimize the chance that a medical device will fail, not just for regulatory testing but throughout its lifetime.
Boosting Medical Innovation
Despite shrinking budgets, leading medical device companies push innovation to the limit, fueled by the demand for new and cheaper medical solutions, an aging population and growing access to care.