At the end of this certificate, students will be able to :
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Master the consequences of the regulatory changes due to the MDR 2017/745 and the IVDR 2017/746 directives, related to medical devices and in-vitro diagnosis
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Display strategic, tactical and communications skills when interacting with Notified Bodies and Authorities, in particular when facing crisis situations
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Display managerial capabilities surrounding production and marketing processes for new medical products
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Develop technical expertise in key topics such as risk management, biocompatibility, usability, clinical investigation and evaluation, and software validation
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Provide management and engineering support during the development projects for new biomedical products