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  1. 1. Developing a guide to regulations forthe Medical Device Industry

    Master-uppsats, KTH/Industriell produktion

    Författare :Sofia Wernquist Örberg; Karl-Fredrik Bergqvist; [2014]
    Nyckelord :;

    Sammanfattning : All Medical devices are required to go through regulatory processes before they can be put on the market. The regulatory processes differ depending on what market is the aim. To release medical devices within the European Economic Area (EEA) the devices need to have a CE marking affixed. LÄS MER