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Health and science

E-cig regulation issues are ‘not black and white’, says FDA’s Zeller

22nd October 2018 - News analysis |

Mitch Zeller, director of the Food and Drug Administration’s Center for Tobacco Products, gave a keynote address at an e-cigarette conference at New York University’s School of Law on Friday. The long-time tobacco hawk struck a surprisingly conciliatory tone, acknowledging that the issue of how to regulate e-cigs, “is not black-and-white,” and that there’s currently “a stalemate” on harm reduction strategies. Zeller also mentioned the Nasem Report, which reported reduced short-term negative health outcomes from e-cigs and that vape users are less likely to smoke cigarettes.

FDA files memo in opposition to public health coalition lawsuit

10th August 2018 - News analysis |

This week, the US Food and Drug Administration (FDA) filed a memo in opposition to a motion for a summary judgment in US District Court in Maryland for a lawsuit against the tobacco deeming extensions. The lawsuit arose from the FDA s defence of its extension of the initial deeming rule compliance deadlines.

FDA squeeze means more bad press for e-cigs

25th May 2018 - News analysis |

E-cigarettes have been hitting the headlines recently, thanks to recent actions by the US Food and Drug Administration (FDA), which has been battling against teen use, particularly Juul Labs’ Juul product. Juul has taken a large portion of the market, and it has been framed as the Pied Piper of e-cigs, supposedly luring teens to the products.

Video: Clearing the clouds: Reduced-risk and vaping regulation

27th April 2018 - Video |

EURACTIV organised a workshop to discuss the way forward in reduced-risk and vaping regulation. Pablo Cano, our head of legal analysis, has participated in the workshop that included the following questions: What are the main differences between e-cigarettes and heated tobacco products? What is the reduced risk potential in this category? What more can be done to ensure a high » Continue Reading.