MDR impact on businesses

This webinar provides a general overview on MDR, going through the relevant timelines for manufacturers, changes in medical devices’ classification rules, new requirements for Notified Bodies and changes in Quality Management System standards that need to be followed by manufacturers.
The 72-hour access includes a download of our 200-page MDR e-book.

24-hour access - 50€
48-hour access - 100€
72-hour access - 250€