51ÁÔÆæ

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In this episode of 51ÁÔÆæ Radio^®, host Brandon Miller is joined by Rod Mell, Executive Head – Life Science Consulting at 51ÁÔÆæ, as well as Jordan Elder, Director of Regulatory both at 51ÁÔÆæ. We explore possible changes in the Medical Device industry in 2025 and provide you with insight on how to prepare yourself for these upcoming initiatives.

Listen in as we go over the updated EU MDR / EUDAMED timelines, recent and upcoming final guidance documents, the strategic priorities outlined by the FDA, the Quality Management System Regulation (QMSR Final Rule), the agency inspection focuses, and how companies can prepare themselves for success with the incoming changes.

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