Azim Chowdhury

Aug 07, 2019 China Is Drafting First E-Cigarette Standard
Oct 12, 2018 Spotlight on Tobacco – Future Developments in the Regulation of Electronic Nicotine Delivery Systems: Potential Over-the-Counter Pathway
Feb 23, 2018 Keller and Heckman LLP Launches Audit and Inspection Program for Vapor and Tobacco Product Manufacturing Establishments
Jan 16, 2018 Hazardous Waste Management Pitfalls for Vapor and E-Liquid Product Manufacturers and Retailers
Dec 12, 2017 Azim Chowdhury Authors Chapter in "Dual Markets - Comparative Approaches to Regulation"
Dec 07, 2017 Dramatic Increase in Proposition 65 Actions Against E-Vapor Products; New Warning Requirements Start August 30, 2018
Nov 29, 2017 FDA to Announce Public Hearing Concerning its Approach to Evaluating the Safety and Efficacy of Nicotine Replacement Therapy (NRT) Products and Formation of a Nicotine Steering Committee
Sep 29, 2017 FDA Extends U.S. Tobacco Product Manufacturing Establishment Registration and Product Listing Deadline to October 12, 2017 to Accommodate Technical Issues with FURLS
Sep 18, 2017 New FDA Guidance Document on Registration and Product Listing for Owners and Operators of Domestic Tobacco Product Establishments Published
Sep 11, 2017 Notice of Appeal Filed in Deeming Rule Challenge by Right to be Smoke-Free Coalition and Nicopure Labs
Aug 14, 2017 10 Business, Advertising, and IP Considerations for E-Vapor Companies
Aug 07, 2017 Azim Chowdhury and Eric Gotting Featured in Vapor Voice Article "Indiana's Vapor Revamp: Following a rebuke in court, Indiana fixes its vapor rules"
Jul 31, 2017 FDA's New Tobacco Strategy: What Does It Mean for Your Vape Business?
May 02, 2017 FDA Delays Upcoming Deeming Compliance Deadlines by Three Months; Sign Up for our FDA Compliance Webinar on May 9, 2017
Apr 25, 2017 New E-Liquid Law Passes in Indiana
Feb 03, 2017 Keller and Heckman LLP Victory for the Right to be Smoke-Free Coalition and E-Vapor Industry in Indiana
Jan 27, 2017 FDA Finalizes New Rule "Clarifying" When a Tobacco Product is Actually a Medical Product
Dec 29, 2016 FDA's Ingredient Listing Deadline Rapidly Approaching for Manufacturers of E-Vapor, E-Liquid and Other Deemed Tobacco Products
Dec 15, 2016 FDA's Establishment Registration and Product Listing Deadline is Fast Approaching - Are You Prepared?
Dec 15, 2016 Revisions to Industry Guidance Regarding FDA Health Document Submission Requirements for Tobacco Products
Nov 01, 2016 Azim Chowdhury Interviewed in VB2B Winter Edition
Aug 17, 2016 FDA Issues Final GRAS Rule; Formally Adopts Voluntary Notification Process
Jul 28, 2016 Right to be Smoke-Free Coalition and E-Vapor Industry Trade Associations file Motion for Summary Judgment in Lawsuit Challenging FDA's Deeming Regulation and the Tobacco Control Act
Jul 13, 2016 New Law on "Liquid Nicotine Containers" Requires Certificates from Each Manufacturer/Importer of E-Liquids
Jun 21, 2016 Right To Be Smoke Free Coalition and E-Vapor Industry Trade Associations File Lawsuit Challenging FDA's Deeming Regulation and the Tobacco Control Act
Apr 29, 2016 The Cole-Bishop Amendment to the Agricultural Appropriations Bill Amending the Grandfather Date for "Deemed" Tobacco Products Passes House Committee - What Next?
Jan 28, 2016 CPSC May Get New Authority Over Liquid Nicotine Containers for E-Cigarettes
Jan 27, 2016 CPSC Likely to Gain New Authority Over Some Nicotine-Containing E-Liquid Packages
Oct 26, 2015 The Grandfather Date – What are FDA's Alternatives?
Oct 23, 2015 FDA Regulation of E-Cigarettes – Are You Prepared?
Jul 13, 2015 "The Deeming Dragon: E-Cigarette Regulation in China"
Nov 20, 2014 Azim Chowdhury Co-Authors FDLI Tobacco Primer
Mar 11, 2014 Keller and Heckman Associate Azim Chowdhury Authors Article in Tobacco Reporter
Sep 22, 2013 Azim Chowdhury Was Quoted in a Recent Article on Electronic Cigarettes
Sep 11, 2013 Azim Chowdhury Authors Article on the Expanding FDA Regulation of Tobacco Products
Mar 05, 2012 FDA Publishes Three New Draft Guidance Documents on Biosimilar Product Development
Apr 20, 2010 Are Electronic Cigarettes Drug Device Combination Products or 'Modified Risk' Tobacco Products?