The FDA’s proposed deeming regulations call for testing of harmful and potentially harmful constituents in electronic cigarettes. Those requirements would not be triggered until three years after the regulations become effective, and in the meantime the FDA presumably would need to establish protocols for e-cigarette testing and a list of constituents to be reported.
Troutman Sanders Tobacco Practice Publishes Article in Smokeshop Magazine on Litigation Over E-Cigarette Marketing
An article by the Troutman Sanders tobacco practice appears in the April issue of Smokeshop Magazine. The article, titled “E-Cigarette Marketing: Misleading or Puffery?,” discusses lawsuits filed by plaintiff’s attorneys against e-cigarette companies regarding their marketing practices. The full text of the article can be found here.
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Report from the Food & Drug Law Institute Conference
We attended the two-day Food & Drug Law Institute Conference this week. Three panels focused on FDA regulation of tobacco products, including a deeming regulations panel at which Bryan Haynes presented.
Troutman Sanders Tobacco Practice Quoted on FDA Deeming Regulations
The Troutman Sanders tobacco practice has been quoted in two recent articles regarding the FDA’s recent move to extend regulatory oversight to e-cigarettes, cigars, pipe tobacco and other tobacco products.
The FDA’s New Deeming Regulations — Get Your Comments In!
The FDA issued proposed regulations yesterday that would extend the FDA’s regulatory authority under the Tobacco Control Act to all tobacco products, including e-cigarettes, cigars and pipe tobacco. It is important to note that this is a proposal only, and the regulations could become more reasonable or more onerous after a public comment period.
The FDA’s New Deeming Regulations– Preliminary Observations — Electronic Cigarettes
FDA’s proposed deeming regulation issued earlier today would cover a variety of products that meet the statutory definition of a “tobacco product,” including electronic cigarettes, cigars and pipe tobacco. This blog entry discusses three provisions that would apply to the tobacco products “deemed” to be subject to FDA regulation.
The FDA’s New Deeming Regulations — Preliminary Observations — Premarket Review / Substantial Equivalence
The FDA’s proposed deeming regulations issued earlier today purport to contain a number of relatively modest proposals for regulation of the newly “deemed” products — generally e-cigarettes, cigars and pipe tobacco. However, lost in the shuffle of the media commentary thus far is the proposal’s impact on tobacco companies’ ability to market new products, or even to continue to market products that are currently being sold.
The FDA’s New Deeming Regulations — Preliminary Observations — Potential Exemption for Premium Cigars
FDA issued the long-awaited deeming regulation this morning. With respect to cigars, FDA proposed two options for the scope of the rule. FDA is requesting comments on the two options, and comments must be submitted within 75 days of the issuance of the proposed rule.
Oklahoma Bill Would Impose Greater Obligations upon Nonparticipating Manufacturers, Wholesalers and Distributors
Nonparticipating manufacturers, wholesalers, and distributors that do business in Oklahoma will be subject to substantial additional requirements if House Bill 2363 currently pending in the Oklahoma State Legislature is enacted. The bill has passed both houses of the Legislature and appears to be headed toward approval.
Troutman Sanders Tobacco Partner Featured in News Report on E-Cigarettes
The television arm of the Washington Post, Post TV, recently ran a news report on electronic cigarettes titled “E-cigs: The battle happening on nicotine’s next front”. The report discusses the recent popularity of e-cigarettes, and speaks of concerns regarding both the impending regulation of the product by the FDA as well as the restrictions that are already beginning to be imposed by major cities on the product.