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This detailed and comprehensive webinar provides an overall analysis of the main changes introduced by MDR, including relevant timelines, new requirements for Notified Bodies and Quality Management Standards, guidance on clinical evidence and clinical evaluation reports, centralisation of the notification through EUDAMED, as well as an overview of the role of the PRRC (Person Responsible for Regulatory Compliance), Authorised Representative, importers and distributors of medical devices. Includes a download of our 200-page MDR e-book.
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