How has EFORT contributed to the implementation of the Medical Device Regulation through CORE-MD?

November 13, 2024 By

Between April 2021 and March 2024, EFORT has been involved as co-leader in an EU-funded project called CORE-MD. CORE–MD objectives were to systematically review methodologies for the clinical investigation of high-risk medical devices (Work Package 1), recommend how new trial designs can contribute (Work Package 2), and advise on methods for aggregating real-world data from […]

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