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US FDA stops notarizing device export certificates, but enhances online application tool

This article was originally published in SRA

Executive Summary

The US Food and Drug Administration has discontinued its practice of notarizing medical device export certificates1 and manufacturers will now have to apply to another government department for the authentication. At the same time, the agency is enhancing its voluntary online system for allowing manufacturers to request export documents more efficiently than by submitting their applications on paper2.

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