100% Discount || Medical Device Regulations

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    Medical Device Regulations

    No prior knowledge of medical device development is required
    Knowledge of basic business practices and project management will be helpful but is not essential
    The medical device industry is growing rapidly, providing great opportunities for innovators, experts and entrepreneurs. This course will provide a detailed overview of the way in which new devices go from concept to product, providing you with a starting point to develop a deep understanding of this complex and fast-moving business space.

    We will cover all of the key components of bringing a new device to market, including:

    Paths to Market, including the 510K, PMA, HDE and other commonly used pathways

    Clinical trials of medical devices, including IDE, submissions, records and reporting

    Risk management and quality in device development

    During this course we will also cover the publicly available information sources that will enable you to research device companies and understand their value. We will cover medical device databases that allow you to research marketed medical devices. We will cover clinic

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