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Compliance Flash: Single Use Devices
Re-use of Single Use Devices can put physicians and manufacturers at risk for health care fraud and adulteration.
Veronica Downen, M.S., RAC
Overview
At MCRA, Veronica leads and supports regulatory projects from regulatory strategy assessments through full submission writing and communications with FDA. These engagements have helped MCRA clients to avoid numerous unnecessary or burdensome processes and have helped streamline costs and timelines on a broad scope of projects.
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