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Regulatory reports

PMTA and MRTP: navigating the path to FDA approval for reduced-risk products

Written by || 14th September 2017 || Regulatory reports , Topic regulatory reports || Regulation and Legislation | North America United States

As PMI’s iQOS comes under consideration by the US FDA, we examine the hurdles it – and other – heated tobacco and e-cigarette products will have to clear to obtain authorisation for commercialisation and reduced-risk claims. ...

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