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Bryan Haynes will moderate a panel entitled FDA implementation of Tobacco Product Pathways.  Panelists, which include the Director of the FDA’s Center for Tobacco Products Office of Science, will discuss the FDA’s implementation of tobacco product review pathways including premarket tobacco applications and modified risk tobacco product applications, as well as impacts on consumers, manufacturers, and tobacco harm reduction efforts.  Panelists will also address opportunities to clarify the implementation of these pathways, including the current status of substantial equivalence applications and the need for a clear set of achievable requirements for product review submissions.

We look forward to seeing our clients and friends at the conference.

 

On Tuesday, April 24 2018, 1:00 – 2:30 PM ET, Bryan Haynes and Paige Fitzgerald will be participating in the American Bar Association webinar, “State and Local Regulations of E-Cigarettes and Other Electronic Nicotine Delivery Systems.” Join our esteemed panel as they:

  • Discuss the current landscape of federal, state, and local regulation of the sale and marketing of e-cigarettes
  • Consider the regulatory environment for new laws and regulations

To learn more about and register for the program, copy the link to visit https://shop.americanbar.org/eBus/Default.aspx?TabID=1538&productId=312520639 . As a member of the faculty I’m able to provide you 10% off your registration rate when you enter this discount code FACMARK at check-out.

Troutman Sanders Partner Bryan Haynes will attend the Food and Drug Law Institute Conference on Enforcement, Litigation, and Compliance held December 6-7, 2017 in Washington, DC. Bryan will moderate a session on the FDA’s enforcement of age verification and other requirements for tobacco products.

Click here to learn more about the conference.

For questions and/or comments, please contact Bryan Haynes, at 804.697.1420 or by email.

 

Tobacco team members Bryan Haynes and Paige Fitzgerald attended this year’s Annual Conference hosted by the Food and Drug Law Institute (FDLI) in Washington, DC, on May 4-5, 2017.  Bryan and Paige covered each of the tobacco-related sessions, and wrote an article for the organization’s Update magazine, which covers current regulatory issues of importance to the industry.  Continue Reading Troutman Tobacco Team’s Article Featured in FDLI’s Update Magazine

Troutman attorney Bryan Haynes will attend this year’s 85th annual IPCPR trade show held July 10-14, 2017 in Las Vegas, NV. You can meet Bryan at the Smokeshop Magazine booth.

Click here to learn more about the IPCPR and the Trade Show.

For questions and/or comments, please contact Bryan Haynes, at 804.697.1420 or by email.

On Thursday, May 4, 2017, Bryan M. Haynes, Partner, Troutman Sanders LLP, will moderate a session on the FDA Center for Tobacco Products’ Evaluation of Premarket and Modified Risk Tobacco Product Applications at the 2017 Food and Drug Law Institute Annual Conference, which will be held in Washington, DC. This session will include a discussion of the FDA’s standards for reviewing premarket tobacco applications, as well as modified risk tobacco applications.