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    Medical devices/medicine

    Zarządzanie księgą jakości

    The program supports the Quality Management System in organizations dealing with the design, production, installation and servicing of medical devices in the field of safety and improving the quality of processes and products, as well as storing and processing documentation, controlling and increasing the competence of employees.

    Standards and requirements: ISO 17025, ISO 13485, ISO 9001

    Functionality: process cards, process mapping, CAPA, training, audits.

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