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BioPharmaceutical

FDA Readies Proposed Rule On Combination Products Postmarket Reporting

This article was originally published in The Pink Sheet Daily

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Executive Summary

A proposed rule wending its way through regulatory review would clarify adverse event reporting requirements for makers of combination products.
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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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