The end of the COVID-era emergency use authorization (EUA) is rapidly approaching - do you know what's next?

Earlier in the year, the FDA laid out their proposed plans for transitioning devices marketed under and EUA or FDA enforcement policy - then went radio silent.

They still haven't released their final guidance, so what's a manufacturer to do?

In this podcast, we'll review the proposed FDA recommendations, suggest the type of feedback industry should provide to the FDA, and discuss actions to take if you are a manufacturer with an active EUA.

In other words, we'll laugh, we'll cry, we'll rail at the insanity that has been the entire EUA process. 😁

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