针对新项目的创新及协作式同步项目管理
汽车及交通运输行业
Integration of mechanical, software and electronic systems technologies for vehicle systems
了解行业应用能源与公用事业
Supply chain collaboration in design, construction, maintenance and retirement of mission-critical assets
了解行业应用Heavy Equipment
Construction, mining, and agricultural heavy equipment manufacturers striving for superior performance
Explore Industry工业机械与重型装备行业
Integration of manufacturing process planning with design and engineering for today’s machine complexity
了解行业应用Insurance & Financial
Visibility, compliance and accountability for insurance and financial industries
Explore IndustryMedia & Telecommunications
Siemens PLM Software, a leader in media and telecommunications software, delivers digital solutions for cutting-edge technology supporting complex products in a rapidly changing market.
Explore IndustrySmall & Medium Business
Remove barriers and grow while maintaining your bottom line. We’re democratizing the most robust digital twins for your small and medium businesses.
Explore IndustryDe-risking medical device development with simulation
De-risking medical device development with simulation
Solutions for every stage, from initial design to regulatory submission
Medical device development is rife with risk at multiple steps of the process, from initial concept to regulatory submission and beyond. For smaller companies, the risks are often more acute, but companies of all sizes have access to a technology that can substantially reduce the risk level at multiple stages of the process: simulation.
This webinar provides an overview of the medical device design and development process, with an emphasis on the areas (and stages) in which simulation can have the most impact, and the kinds of simulation tools that provide device developers the ability to minimize risk while maximizing performance.
Innovations in medical devices come from companies of all sizes. Thanks to simulation, companies of any size have access to tools that help them predict the performance of their devices and can even provide more detail and insight than physical tests allow.
There are simulation solutions for each design stage (preliminary design through to detailed design) and for each scope (design of individual components or complete systems) for all the groups involved—designers, analysts, R&D. And as regulatory bodies increasingly support the use of simulation data in regulatory submissions, the role and value of simulation (along with the importance of managing simulation data) keeps increasing.
This webinar features a conversation between Portfolio Development Executive Alexandra Francois-Saint-Cyr and Koen Beyers, the Founder of Voxdale and CTO of Novosanis. Koen summarizes the value of simulation this way: “At both companies early verification in a stringent design control process is key to decrease Time to Market and master the full product lifecycle of medical devices."
您好,鲍勃(将会在访问实际网站时替换为真实名字)
我们想要了解更多有关您的信息。
页面提交出错。请重新尝试。
首次订阅 Siemens Digital Industries Software 电子邮件?稍后您将收到一封电子邮件,请务必点击确认,以完成订阅。
您好,鲍勃(将会在访问实际网站时替换为真实名字)
本场网络研讨会将对您开放 90 天。请单击下方开始观看。
Solutions for every stage, from initial design to regulatory submission
Medical device development is rife with risk at multiple steps of the process, from initial concept to regulatory submission and beyond. For smaller companies, the risks are often more acute, but companies of all sizes have access to a technology that can substantially reduce the risk level at multiple stages of the process: simulation.
This webinar provides an overview of the medical device design and development process, with an emphasis on the areas (and stages) in which simulation can have the most impact, and the kinds of simulation tools that provide device developers the ability to minimize risk while maximizing performance.
Innovations in medical devices come from companies of all sizes. Thanks to simulation, companies of any size have access to tools that help them predict the performance of their devices and can even provide more detail and insight than physical tests allow.
There are simulation solutions for each design stage (preliminary design through to detailed design) and for each scope (design of individual components or complete systems) for all the groups involved—designers, analysts, R&D. And as regulatory bodies increasingly support the use of simulation data in regulatory submissions, the role and value of simulation (along with the importance of managing simulation data) keeps increasing.
This webinar features a conversation between Portfolio Development Executive Alexandra Francois-Saint-Cyr and Koen Beyers, the Founder of Voxdale and CTO of Novosanis. Koen summarizes the value of simulation this way: “At both companies early verification in a stringent design control process is key to decrease Time to Market and master the full product lifecycle of medical devices."