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FDA Regulation United States

Some Long-Standing FDA Regs Face Mandatory Review Or Rescission Under New HHS Rule

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Executive Summary

Among those judged eligible are FDA rules governing adverse event reporting and the Unique Device Identification System.

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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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