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  1. ライフサイエンス&ヘルスケア
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  3. 3DS
  1. Engineered to Cure

Engineered to Cure

Develop safe and effective medical devices with collaborative design and simulation

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The increasing global incidence of chronic diseases demands that novel solutions be developed rapidly and within tight budgets, yet be safe and efficacious enough to withstand stringent regulatory scrutiny. Moreover, the expectation of measurable long term improvement in patient outcomes is driving the need for greater personalization of therapies. Last but not least, intense competition from traditional and non-traditional players is pushing medical device firms to develop agile product portfolios and processes that can respond to unmet patient needs in a market landscape characterized by constant and rapid scientific, technological, social, and economic change.

The Engineered To Cure industry solution answers these challenges by offering a data-driven & model-based engineering platform that facilitates collaborative design and development of medical devices using best in class apps and processes for 3D design, systems engineering, multiphysics simulations, and virtual human modeling. Using this solution, designers and engineers can rapidly explore the device design space, virtually test promising designs in real world usage scenarios, and validate optimal designs against product requirements and business objectives, while reducing their reliance on expensive and time-consuming physical, animal, and human testing.

Engineered to Cure のベネフィット

  • Increase the range and value of novel medical devices satisfying unmet patient needs

    • Increase innovation bandwidth and success rate through collaborative use of validated models and methods
    • Virtually validate device mechanical performance using regulatory grade models
    • Assess performance and safety of smart connected medical devices
    • Rapidly explore device and patient variability to optimize device performance for individuals and populations
  • Reduce cost and time of new product development

    • Implement fully integrated and standardized simulation-driven design processes and methods and democratize them to a broader user community
    • Plan and execute optimal device performance verification and validation strategy
    • Automatically develop and maintain complete traceability and defensibility from requirements through certification
    • Minimize the need for benchtop, animal, and human testing
  • Improve patient experience and treatment outcome

    • Assess device safety and efficacy in a realistic virtual human environment
    • Develop validated personalized and population human models
    • Enable early stage virtual evaluation of patient, caregiver, and practitioner experience
    • Deploy a systematic approach to design robust, safe, and personalized medical devices