Date of publication: June 2020
60,00€ excl. VAT
We clarify for you frequent misconceptions on the requirements and provisions of the MDR, and provide you with all the answers in a user-friendly manner.
25-page long document covers topics of legacy devices & applicable dates, obligations of economic operators & QMS, PRRC, Basic UDI-DI & UDI requirements, clinical evaluation, post-market surveillance obligations & needed reports, grace period, EMDN and more!