Virtonomy GmbH

Virtonomy aims to transform medical device development by providing a virtual environment for testing and optimization, ultimately leading to safer and more effective devices.

Founded: 2019 Headquarters:Paul-Heyse-Straße 6 ,80336

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  • Non-Provider Industry Solutions
  • Accelerate clinical trials with digital patient twins, ensure their success, reduce costs and time

    Virtonomy’s v-Patients software allows medical device developers to conduct development and testing within a virtual environment. The solution leverages a comprehensive digital twin and simulation platform built on a continually growing database of real clinical data, accurately representing anatomical differences, demographic diversity, and various pathological conditions.

      • Digital Patient Twins: Virtonomy offers a database of digital patient models created from real clinical data, including anatomical variability and pathological conditions.

        Virtual Environment: Users can simulate medical device implantation and performance in a virtual environment to optimize design and ensure safety.

         

        Key Features:

        Interactive Implantation: Perform virtual device fitting and measurements.

        Statistical Analysis: Access extensive statistics and worst-case anatomies.

        Regulatory Support: Generates digital evidence for regulatory compliance.

      • Streamlined Development: Reduces development time and costs.

        Improved Safety: Enhances device safety through virtual testing.

        Regulatory Compliance: Supports compliance with FDA and European Commission standards.

      • 2022
    • Clinical Reference
    • Clinicians, Researcher
    • Released
    • Software and Apps
    • Clinical Trials
    • Research
      • Regulatory viewpoint:

        The FDA and European Commission show strong support for virtual patients and simulation.

         

        "FDA’s Office of Science and Engineering Laboratories (OSEL) has committed significant resources for transforming computational modeling from a valuable scientific tool to a valuable regulatory tool because of its potential for significant cost-savings in evaluating medical devices, simulating performance under scenarios that may not be possible with human use or that could more effectively be evaluated with simulation." (Source)



        More useful links:

        FDA’s support on computational modeling

        FDA: Diverse racial and ethnic groups for clinical trials

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    V-Patients

    By: Virtonomy GmbH

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