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US Government Shutdown – What FDA can still be doing?
US Government Shutdown – What the FDA Can Still Be Doing?
When the U.S. government experiences a shutdown, the consequences ripple across every industry — but for medical device manufacturers, the uncertainty can be alarming.
In this article, Regulatory Expert Rob Packard explores what happens to the U.S. Food and Drug Administration (FDA) during a shutdown, and how it affects global manufacturers.
You’ll learn:
Which FDA activities continue, and which are suspended
How submissions like 510(k), PMA, and De Novo are impacted
What happens to clinical trials, recalls, and ongoing investigations…
The skinny
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