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Satyajit Ketkar

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Satyajit Ketkar talks about upcoming changes to the EU MDR regulation and what it will mean for your teams.

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An Interview with Velentium: How Medical Device Developers Can Prepare for EU MDR

on February 11, 2020 / in Compliance & Regulation / by Satyajit Ketkar

EU MDR which emphasizes patient safety, traceability, and transparency, will impact medical device developers, manufacturers, and suppliers across Europe.

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