Avoid pitfalls, unpack issues, and brainstorm solutions for a smoother SE

Join as our panel provides firsthand knowledge to help you navigate the exacting requirements of the FDA’s Center for Tobacco Products’ SE process with best practices, common and not so common pitfalls, and the opportunity to engage with peers who are fully immersed in the process.  

Location: Residence Inn by Marriott - Raleigh Durham Airport/Morrisville

2020 Hospitality Court

Morrisville, NC

 

 

  In-Person Company-Wide Virtual Combo
  $299 $499 $999
Networking and one-to-one interaction with speakers and attendees  
On-site lunch and networking  
Engage with real-time Q&A
Convenient at-your-desk access to live workshop  
Single registration for company-wide virtual access   
In-Person attendees 1 - 3
 
 
Contact us for special rates offered to academia and government organizations
 
Moderator

Beth Oliva

Fox Rothschild

Speakers

Kim Hesse 

Global Laboratory Services

Sarah Evans

Turning Point Brands

Patrick Murphy RAI Services

Darren DeSoi 

Scandinavian Tobacco Group 

Frank Herrera 

H New Media Law 

Paisley Cameron

JTI - USA  

Topics

Overview of the SE Process

What We Have Learned from Originally Regulated Products and What We Don’t Know

  • Role of Grandfather Requests
  • SE Exemptions
    • What is it?
    • How to Use This Pathway
  • SE Reports
  • Predicate Issues
  • Content Issues
  • Environmental Impact Analysis

What Happens (or Should Happen) After You Submit an SE Report

Have questions? Need more info? Contact Michelle Parisi via phone at 919 504-5491 or email at michelle@tma.org