Join a diverse group of stakeholders – public health advocates, researchers, manufacturers, lawyers, consumer interest groups, entrepreneurs, governmental agencies, and others – for this two-day conference on effectively regulating the broad spectrum of tobacco and nicotine products in the US. Attendees will hear directly from FDA about the latest updates on regulations, guidance documents, and other initiatives. The conference will also include numerous discussions of timely tobacco and nicotine product issues and feature interactive dialogues between the panelists and audience.

Recent Premarket Tobacco Application (PMTA) Decisions, Marketing Denial Order (MDO) Litigation, and Protecting CTP Decisions from Future Legal Challenges - 11:20 am – 12:30 pm

Moderator: Bryan M. Haynes, Partner, Troutman Pepper Hamilton Sanders LLP

Panelists:

• Beth G. Oliva, Partner, Fox Rothschild LLP
• Connor Fuchs, Senior Staff Attorney, Campaign for Tobacco-Free Kids
• Eric N. Heyer, Partner, Thompson Hine LLP
• Eric N. Lindblom, Independent Consultant and Senior Scholar, O’Neill Institute, Georgetown Law Center

State and Local Regulatory Developments and Enforcement Challenges - 9:00 am – 10:20 am 

Moderator: Barry Schaevitz, Partner, Fox Rothschild LLP

Panelists:

• Michael Hering, Director, Center for Tobacco and Public Health & Chief Counsel, National Association of Attorneys General
• Agustin Rodriguez, Partner, Troutman Pepper Hamilton Sanders LLP
• Kevin R.J. Schroth, Associate Professor, Rutgers School of Public Health

Please note there is a cost to attend. CLE credits are available.