The Troutman Sanders Tobacco Team will attend the FDLI Tobacco and Nicotine Products Regulation and Policy Conference on October 24-26, 2018. The conference will feature a diverse group of stakeholders – manufacturers, governmental agencies, researchers, public health advocates and attorneys – discussing the effective regulation of tobacco and nicotine products in the U.S. and globally. The FDA’s Center for Tobacco Products Director Mitch Zeller will speak about the latest updates on regulations, guidance and other initiatives. Continue Reading Troutman Sanders Tobacco Team to Attend Food and Drug Law Institute Tobacco Conference
Bryan Haynes of the Troutman Sanders Tobacco Team will be at the International Premium Cigar and Pipe Retailers Trade Show from July 13-15. We look forward to seeing our clients and friends at the show.
On April 24, 2018, Troutman attorneys Bryan Haynes and Paige Fitzgerald presented an American Bar Association webinar on the regulations of e-cigarettes and other Electronic Nicotine Delivery Systems (ENDS).
You may purchase the recording of Bryan and Paige’s seminar here.
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 Tobacco Team leader Bryan Haynes will be in attendance at the 2018 Tobacco Plus Expo in Las Vegas. The trade show is January 31 to February 1, and brings together many of the top brands in the tobacco and vapor products industries. We look forward to seeing our clients and friends at the show.
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.
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.
Troutman Sanders Partner, Bryan M. Haynes, to attend the 102nd annual Tobacco Manufacturers Association conference held in Chantilly, VA from May 10-12, 2017. Noteworthy sessions to include Navigating Premarket Authorization & Harm Reduction… and Testing Methodologies for Deemed Products.