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Regulatory reports

The deeming rule and PMTAs: what it all means for manufacturers

Written by || 26th June 2016 || Regulatory reports , Topic regulatory reports | Health and science | Nicotine | Policy and Politics | Regulation and Legislation | North America United States

Contents1 Introduction2 Why an ENDS product requires FDA approval3 Pathways to approval4 The FDA guidance on PMTAs5 PMTAs, public health, and scientific studies     There may be more recent ECigIntelligence reports on this territory. Please visit the home page for the United States or the advanced search page.       Introduction   On 10th May, the U.S. Food and Drug Administration (FDA) » Continue Reading.
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Aidan Semmens

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