FDA Extends Deadlines for E Cig, E Liquid & ENDS Compliance


The FDA has extended the deadlines for compliance of the new deeming regulations for e cigarettes, e liquid and ENDS products!  The have announced a 3 month extension of certain tobacco product compliance deadlines.  Manufacturers now have  additional time to comply with new CTP provisions such as: Submission of cigar rotational warning plans Registration and [ ] The post FDA Extends Deadlines for E Cig, E Liquid & ENDS Compliance appeared first on Brown & Charbonneau, LLP.
http://www.bc-llp.com/fda-extends-deadlines-e-cig-e-liquid-ends-compliance/

Guidance from FDA About the Pre Market Tobacco Application (PMTA) Process


Guidance from FDA About the Pre Market Tobacco Application (PMTA) Process The US Food and Drug Administration (FDA) deemed all “tobacco products” within its authority and subject to the Tobacco Control Act (TCA). FDA has made available extensive information regarding tobacco products and the new regulations. With regard to selling newly deemed tobacco products, manufacturers those products that [ ] The post Guidance from FDA About the Pre Market Tobacco Application (PMTA) Process appeared first on Brown & Charbonneau, LLP.
http://www.bc-llp.com/guidance-fda-pre-market-tobacco-application-pmta-process/

FDA Compliance Deadlines for E Liquid & E Cig Manufacturers (Updated)


FDA Compliance Deadlines for E Liquid & E Cig Manufacturers July 26, 2016 Child-Resistant Packaging Nicotine provided in a liquid nicotine container that is sold, offered for sale, manufactured for sale, distributed in commerce, or imported into the United States must be packaged in accordance with the poison prevention packaging standards issued by the Consumer [ ] The post FDA Compliance Deadlines for E Liquid & E Cig Manufacturers (Updated) appeared first on Brown & Charbonneau, LLP.
http://www.bc-llp.com/fda-compliance-deadlines-e-liquid-e-cig-manufacturers/

FDA Extends Deadline for Submission of Ingredient Listings for E Cig & E Liquid Manufacturers


FDA Extends Deadline for Submission of Ingredient Listings for E Cig & E Liquid Manufacturers In the FDA s revised guidance for submission of listing of ingredients for tobacco products, the FDA is announcing an additional 6-month compliance policy for newly deemed tobacco products on the market as of August 8, 2016. Under this policy, FDA [ ] The post FDA Extends Deadline for Submission of Ingredient Listings for E Cig & E Liquid Manufacturers appeared first on Brown & Charbonneau, LLP.
http://www.bc-llp.com/fda-extends-deadline-submission-ingredient-listings-e-cig-e-liquid-manufacturers/

FDA Extends Deadline for E Cig Manufacturing Registration from 12/31/16 to 6/30/16


FDA Extends Deadline for E Cig Manufacturing Registration from 12/31/16 to 6/30/16 Registration and Listing Guidance Revised with New Compliance Period Click Here to Read Revised Guidance Today, the FDA issued the revised guidance, “Registration and Product Listing for Owners and Operators of Domestic Tobacco Product Establishments.” In the initial revised guidance issued in July [ ] The post FDA Extends Deadline for E Cig Manufacturing Registration from 12/31/16 to 6/30/16 appeared first on Brown & Charbonneau, LLP.
http://www.bc-llp.com/fda-extends-deadline-e-cig-manufacturing-registration-123116-63016/

US Senator Warns FDA that Congress will Target New E Cig Regulations


US Senator Warns FDA that Congress will Target New E Cig Regulations The Winston-Salem Journal reports: U.S. Sen. Ron Johnson, R-Wisconsin sent a letter Tuesday to FDA Commissioner Robert Califf that warns him that a Republican-controlled Congress and White House will target some, if not all, of the regulations that went into effect Aug. 8 [ ] The post US Senator Warns FDA that Congress will Target New E Cig Regulations appeared first on Brown & Charbonneau, LLP.
http://www.bc-llp.com/us-senator-warns-fda-congress-will-target-new-e-cig-regulations/

Quick Summary of New FDA E Cig Label Requirements


Here is a Quick Summary of New FDA E Cig Label Requirements.  These apply to anyone who manufactures, packages, sells, offers to sell, distribute or import for distribution of e cigarettes, e liquid and other tobacco products .  For all information on FDA deeming regulations, click here. ·      State the name and place of business of manufacturer [ ] The post Quick Summary of New FDA E Cig Label Requirements appeared first on Brown & Charbonneau, LLP.
http://www.bc-llp.com/quick-summary-new-fda-e-cig-label-requirements/