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Risk Analysis in MR Medical Device Trials

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Published 01.06.2025By Johannes Slotboom
Categorized as Ethics Proposal-Related Writing, Risk management, Swissmedic/EMA Proposal-Related Writing, Uncategorized Tagged dual tuned RF head coil, EMA, IEC 60601-2-33, ISO 14155, missing CE-marking, Risk management, Swissmedic

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  1. Pingback: How to Apply for a Swissmedic Approval for your MR-research – MRI/MRS Clinical Trial Compliance Solver
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