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US FDA to hold workshop on device postapproval studies

This article was originally published in RAJ Devices

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Executive Summary

The US Food and Drug Administration is organising a public workshop to facilitate discussion among stakeholders on methodologies for postapproval studies of medical devices1,2.

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This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

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