FDA Regulation of Tobacco Products: The Deeming Regulation - Impact on E-Cigarettes

This webinar on tobacco regulations will discuss FDA regulatory requirements for tobacco products. It will prepare you for FDA’s Deeming Regulations for cigars, pipe tobacco, electronic cigarettes, dissolvable tobacco and other novel tobacco products.

Why Should You Attend:

FDA recently released proposed regulations that would bring tobacco products not currently regulated by the FDA under the control of the Tobacco Control Act (the so-called ‘Deeming Regulations’). This rule will substantially change the way e-cigarettes, cigars, and other tobacco products are currently manufactured, marketed and distributed.

This 60-minute webinar will focus on key points of the Deeming Regulations, discuss the provisions of the rule on which the FDA requested public comment, discuss the potential public health impact and explore the varying stakeholder perspectives. It is critical for manufacturers and importers of cigars, pipe tobacco, electronic cigarettes, dissolvable tobacco and other novel tobacco products to be prepared to comment on Deeming Regulation by August 8, 2014.

Areas Covered in the Webinar:

• History - What led to the Deeming Regulation
• Key Provisions of the Deeming Regulation
• Impact on pipe tobacco, dissolvable tobacco and other novel tobacco products
• Impact on the Electronic Cigarette Industry
• Important Arguments to Make in your Public Comments

Who Will Benefit:

• General Counsel and Management of tobacco companies, e-cigarette companies, etc.
• Regulatory Compliance Associates and Managers
• Medical professionals, public health and consumer advocates, and other individuals working in the smoking control/harm reduction area
• Regulatory affairs professionals and scientists who work in this area
• Manufacturers and importers of e-cigarettes and other novel tobacco products
• Suppliers to Tobacco Industry