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Medical Device

When Communicating Product Risks, FDA Should Involve Firms – AdvaMed

This article was originally published in The Gray Sheet

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Executive Summary

AdvaMed is urging FDA to "routinely" consult with manufacturers when developing and evaluating safety-related communications about devices, drugs and other regulated 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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