The global regulatory environment for tobacco, e-cigarette and e-liquid products is rapidly evolving as legislators and regulators in the United States, European Union and Asia attempt to understand the health and safety concerns presented by these novel products, and develop appropriately tailored laws and regulations. This training course will present an overview of e-cigarette regulations in Asia, the European Union and around the world. It will also detail the key provisions of FDA’s deeming regulations.
Why Should You Attend:
This session will review the legal status of these products in the United States, European Union, Asia and around the world, with a focus on the impact of the new deeming regulations recently published by the FDA, which propose to treat e-cigarettes and their components as tobacco products. Join Mr. Chowdhury, who is a thought-leader in this field and represents numerous e-cigarette industry stakeholders in matters of regulatory compliance, in a discussion on how FDA’s proposed rule will substantially change the way e-cigarettes are currently manufactured, marketed and distributed in the United States, as well as its potential impact on the global market.Areas Covered in the Webinar:
- Overview of e-cigarette regulations in Asia, European Union and around the world
- History - what led to U.S. FDA’s deeming regulation
- Key provisions of the deeming regulation
- Impact on the electronic cigarette industry
- How manufactures in China and around the world can prepare to comply
Who Will Benefit:
- General counsel and management of tobacco, e-cigarette and e-liquid companies
- 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 for the tobacco and e-cigarette industries
Course Provider
Azim Chowdhury,
