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Regulatory reports

Relabelling and repackaging options could ease legal burden for US manufacturers

Written by || 24th April 2018 || Regulatory reports , Topic regulatory reports | FDA | Health and science | Marketing and Retailing | Policy and Politics | Regulation and Legislation | GeographiesNorth America United States Washington

There could be some relief for manufacturers of “tobacco related” products for the US market who have been restricted by the complicated legal process of obtaining authorisation from the US Food and Drug Administration (FDA) in the form of a premarket tobacco product application (PMTA).
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Aidan Semmens

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