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FDA releases notification requirements to protect medical device supply chains

February 4, 2022 By Danielle Kirsh

Emergo-UL-logoBy Stewart Eisenhart, Emergo Group

The FDA has published new guidance on reporting and notification requirements to better mitigate supply disruptions when medical device manufacturers cease or suspend production during public health emergencies.

Get the full story here at the Emergo Group’s blog.

The opinions expressed in this blog post are the author’s only and do not necessarily reflect those of MedicalDesignandOutsourcing.com or its employees.

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  • Medical Device Business
    • Mergers & Acquisitions
    • Financial
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  • Applications
    • Cardiovascular
    • Devices
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    • Orthopedic
    • Surgical
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    • Contract Manufacturing
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    • Extrusions
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    • Motion Control
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