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FDA demands health documents from U.S. makers and importers

Written by || 18th October 2016 || Regulatory reports , Topic regulatory reports || Health and science | Regulation and Legislation | North America United States

Following the introduction this summer of the deeming regulations by the U.S. Food and Drug Administration (FDA), each vapour product manufacturer or importer is required to submit health documents describing the physiological, behavioural and toxicological effects of their tobacco products, current or future. ...

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