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  Tissue Simulation: Advances for Next-Gen Medical Devices

  Today, 85% of the top 50 healthcare companies use Computational Modeling and Simulation (CM&S) to develop their products and processes. Whether it’s refining overall device parameters or optimizing critical requirements, engineering simulations help reduce development timelines and enhance design exploration.

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  Regulatory Clearance through Computational Simulation: Industry Opinion, FDA Strategy, & Successful Case Studies

  Computational Modeling and Simulation (CM&S) for medical devices has become a pivotal tool across the medical device industry, complementing and often enhancing traditional bench testing and clinical studies.

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  Computational Modelling and Simulation in Medical Device Development

  In a sophisticated world of ever increasing complexity, we need our tools to evolve alongside us and assist in complex decision making, allowing us to understand the consequences of choices ahead. Computational Modelling and Simulation (CM&S) is emerging as an essential tool in building evidence for medical device development.

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  Developing Optimized Aerosol Drug Delivery Systems

  Aerosol Drug Delivery Systems, including Aerosol-based pulmonary-delivered drug devices, offer significant value by enabling targeted drug delivery directly to the respiratory system.

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  Medical Device Vibration Analysis and Testing Reduce Risk

  The impact of vibration on medical devices can be understood through a combination of vibration analysis and testing. This article reviews medical devices most susceptible to vibration, provides basic theory and methods of vibration analysis, and summarizes the benefits of using modal analysis when developing medical devices.

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  Use computational modeling to validate thermoplastic properties in medical device design

  Importance of using Computational modeling thermoplastic properties to predict and validate thermoplastic properties in a medical device.

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  In Silico Medical Device Drop Testing VS Benchtop

  In silico medical device drop testing offers scalability, fast-tracking of iterations, and the ability to review hard-to-detect failure modes.

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  3D Printed Parts Streamline Development Process

  3D Printed Parts Streamline Development provides context for designers using 3D printed parts as a part of their market-ready medical devices.

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  3D Printed Medical Devices – Insight into the FDA Guidance on Additive Manufacturing

  FDA Guidance on Additive Manufacturing (AM) – offers new ways to integrate parts not only for prototypes, but for final products.

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