2014 - FDA Regulation on Tobacco Products, Deeming regulations and Impact on E-Cigarettes
Date2014-09-19
Deadline2014-09-19
VenueVirtual Webinar, USA - United States
KeywordsFda deeming regulation; Fda tobacco regulation; Tobacco Control Act
Topics/Call fo Papers
Instructor: Azim Chowdhury
Description:
The webinar on FDA Regulation on Tobacco Products, Deeming regulations & Impact on E-Cigarettes will mainly focus on Tobacco Control Act, impact of tobacco products.
This 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. FDA recently released 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.
The Food and Drug Administration (FDA) has now proposed to deem products meeting the statutory definition of "tobacco product," except accessories of a proposed deemed tobacco product, to be subject to the Federal Food, Drug, and Cosmetic Act (the FD&C Act), as amended by the Family Smoking Prevention and Tobacco Control Act (Tobacco Control Act). The Tobacco Control Act gives FDA the authority to regulate the manufacture, labeling, distribution, and marketing of tobacco products in the United States.
FDA also is proposing to prohibit the sale of "covered tobacco products" to individuals under the age of 18 and to require the display of health warnings on cigarette tobacco, roll-your own tobacco, and covered tobacco product packages and in advertisements.
Why Should you Attend:
This webinar will present a brief History on What led to the Deeming Regulation and a detailed explanation on FDA Regulation on Tobacco Products, Deeming regulations & Impact on E-Cigarettes.
Objectives of the Presentation:
To showcase the Key Provisions of the Deeming Regulation.
To give a detailed insight on the 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
General Counsel and Management of tobacco companies, e-cigarette companies, etc.
Who can Benefit:
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.
Quick Contact:
---
http://www.onlinecompliancepanel.com/ecommerce/web...
Toll free: +1-510-857-5896
Email:?webinar-AT-onlinecompliancepanel.com
OnlineCompliancePanel LLC,
38868 Salmon Ter,
Fremont, CA 94536, USA
Description:
The webinar on FDA Regulation on Tobacco Products, Deeming regulations & Impact on E-Cigarettes will mainly focus on Tobacco Control Act, impact of tobacco products.
This 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. FDA recently released 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.
The Food and Drug Administration (FDA) has now proposed to deem products meeting the statutory definition of "tobacco product," except accessories of a proposed deemed tobacco product, to be subject to the Federal Food, Drug, and Cosmetic Act (the FD&C Act), as amended by the Family Smoking Prevention and Tobacco Control Act (Tobacco Control Act). The Tobacco Control Act gives FDA the authority to regulate the manufacture, labeling, distribution, and marketing of tobacco products in the United States.
FDA also is proposing to prohibit the sale of "covered tobacco products" to individuals under the age of 18 and to require the display of health warnings on cigarette tobacco, roll-your own tobacco, and covered tobacco product packages and in advertisements.
Why Should you Attend:
This webinar will present a brief History on What led to the Deeming Regulation and a detailed explanation on FDA Regulation on Tobacco Products, Deeming regulations & Impact on E-Cigarettes.
Objectives of the Presentation:
To showcase the Key Provisions of the Deeming Regulation.
To give a detailed insight on the 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
General Counsel and Management of tobacco companies, e-cigarette companies, etc.
Who can Benefit:
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.
Quick Contact:
---
http://www.onlinecompliancepanel.com/ecommerce/web...
Toll free: +1-510-857-5896
Email:?webinar-AT-onlinecompliancepanel.com
OnlineCompliancePanel LLC,
38868 Salmon Ter,
Fremont, CA 94536, USA
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Last modified: 2014-09-16 18:25:16