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Medical Device User Fee Program (MDUFA IV) › Emergency Use Authorization (EUA)

Womble Bond Dickinson

FDA Suspends Review for Non-COVID-19 In Vitro Diagnostics (IVD) Submissions and Expects Review Delays in Non-IVD Products

Womble Bond Dickinson on

A year into the current public health emergency, the FDA’s Center for Devices and Radiological Health (CDRH) announced on Thursday, April 15, 2021, that the center is “prioritizing and triaging our work using existing...more

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