Digital Evidence Generation: Simulation and the Digital Twin for Better Medical Device Design, New Webinar Hosted by Xtalks

Xtalks Life Science Webinars

In a live broadcast on Friday, February 23, 2018, at 11 a.m. EST (4 p.m. GMT), experts from Siemens PLM including Dr. Kristian Debus, Medical Devices Industry Specialist, and Dr. Tom Phillips, Director of Simulation Portfolio Development, will discuss how digital evidence generation and digital evidence submission will enable medical device companies to improve product engineering practice, drive design excellence, and reduce the time to clearance.

The potential for proactive use of simulation and CAE in medical devices is huge: saving lives and saving millions of dollars for the industry. This could be accomplished by optimizing designs for performance and reliability, reducing the number of required benchtop tests and clinical trials, as well as accelerating the regulatory approval process. Successfully employing simulation forms the fundamental basis for a sound product engineering practice and drives design excellence. The FDA and regulatory agencies worldwide are supporting efforts to use simulation in streamlining the regulatory process through interactions with industry, academics, and consortia like the MDIC (Medical Device Innovation Consortium), or organizations like ASME or Avicenna.

Digital evidence generation is a term coined during a meeting between Siemens PLM and the FDA in October 2017. It describes the process of generating data required for regulatory reporting through digital technologies for digital evidence submission. This then ties into the overall digital enterprise through the use of a digital twin and product lifecycle management over the full product lifecycle. Digital evidence generation and digital evidence submission provide the means to reduce clinical trial costs by offloading animal and human trials to their digital twins and set the stage for a revolution in medical device design.

This webinar is applicable to medical device engineers, designers, R&D technical staff and clinical trial responsible persons. For more information about this free session visit: Digital Evidence Generation: Simulation and the Digital Twin for Better Medical Device Design.

ABOUT XTALKS

Xtalks, powered by Honeycomb Worldwide Inc., is a leading provider of educational webinars to the global life science, food, and medical device community. Every year thousands of industry practitioners (from life science, food, and medical device companies, private & academic research institutions, healthcare centers, etc.) turn to Xtalks for access to quality content. Xtalks helps Life Science professionals stay current with industry developments, trends, and regulations. Xtalks webinars also provide perspectives on key issues from top industry thought leaders and service providers.

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For information about hosting a webinar visit http://xtalks.com/sponsorship.ashx

Contact:

Nima Rajan

Tel: +1 (416) 977-6555 ext 352

Email: nrajan@xtalks.com

Source: Xtalks

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Categories: Electronics, Engineering, Healthcare and Medical Informatics, Material Sciences, Diagnostics, Radiology and Medical Imaging

Tags: engineering, medical device design, regulatory compliance, Siemens, Xtalks


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Xtalks is a leading provider of educational webinars to the global life science, food and medical device community.