Please find the session links next to their corresponding agenda item.

Tuesday, October 17

10:00 AM–11:20 AM 

FDLI Welcome and First Session

FDLI Welcome and Announcements
Bianca Cardona Melendez, Assistant Director, Educational Programs, FDLI

I. The Family Smoking Prevention and Tobacco Control Act (TCA), the Deeming Regulation and Synthetic Nicotine Authority
Vanessa Fulton, Associate, Kleinfeld, Kaplan & Becker, LLP

Enter this session:

11:30 AM–12:30 PM 

II. Pathways to Market and Related FDA Processes
Elizabeth Oestreich, Senior Vice President, Regulatory Compliance, Greenleaf Health, Inc.

Enter this session:

12:30–1:00 PM 


1:00–1:30 PM 

III.  The Public Health Standard
Maham Akbar, Director, Public Policy, Truth Initiative

Enter this session:

1:40–2:40 PM 

IV.  Product Compliance
Philip Langer, Associate, Fox Rothschild LLP

Enter this session:

2:40–3:00 PM


3:00–3:50 PM

V.  FDA Inspections and Enforcement
Benjamin K. Wolf, Senior Associate, Alston & Bird LLP

Enter this session:

4:00–5:00 PM

VI.  Hot Topics and Current Issues Panel Discussion
Kellsi Booth, Vice President, Regulatory Affairs, Turning Point Brands, Inc.
Vanessa Fulton, Associate, Kleinfeld, Kaplan & Becker, LLP
Barry S. Schaevitz, Partner, Fox Rothschild LLP

Enter this session:

5:00 PM


CLE Information


This event is pending approval in Ohio. To obtain credit, please email [email protected] at the end of the conference and include your state bar number along with how many credits you wish to obtain. FDLI will certify your attendance for you. An evaluation is required to obtain credit.


This event is pending approval in Virginia. Please email [email protected] to request a Virginia form. You will need to certify your attendance online at Retain the Certificate of Attendance for two years.

Other States

These CLE approvals may also be honored by other states; please check with your bar association for guidance. At the end of the conference, please email [email protected] to receive a certificate of attendance.