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Electronic Submissions, Modular PMAs Lighten Cardio Division Workload

This article was originally published in The Gray Sheet

Executive Summary

Electronic submissions and modular premarket approval applications are helping ease the backlog in FDA's Cardiovascular, Respiratory and Neurological Devices Division Director Thomas Callahan, PhD, told attendees of the Health Industry Manufacturers Association's Device Submissions Workshop July 28 in Washington, D.C.
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