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User Fee Acts
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Virginia Bio, along with virtually all of the biopharmaceutical and medical device industry, encouraged and supported the creation of several user fee acts a decade ago, to provide FDA additional resources directly from industry users which would be used hire additional experts and reviewers and strengthen and streamline the review process. By all accounts, these User Fee Acts have been successful, and we continue to support them. They were renewed in 2017 in the FDA Reauthorization Act, which was supported by Virginia Bio.

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