The Food Enforcement and Compliance Conference brings leading regulators, attorneys, industry representatives, litigators, academics, and consultants together to discuss the increasing attention on food and dietary supplement regulation, including the latest developments and issues in enforcement and compliance, such as current FDA and USDA/FSIS enforcement priorities, inspection policies, and recent enforcement actions involving alleged violations of food safety or labeling requirements. This conference offers an important opportunity to delve into the latest trends and guidance concerning both enforcement risk factors and strategies for ensuring compliance and minimizing legal risk in the current environment.

Conference Topics:

  • Inspections, Warning Letters, and Compliance
  • Managing Recalls
  • Innovative Foods
  • The Next Phase of Class Actions
  • Criminal Enforcement
  • Supply Chain Verification

Keynote Speaker: 

  • Frank Yiannas, Deputy Commissioner for Food Policy and Response, Office of the Commissioner, FDA

Attendees will:

  • Explore the latest trends behind enforcement actions in food and dietary supplements
  • Gain practical tips and best practices for succeeding during FSMA inspections
  • Learn how to comply with new and upcoming FDA rules and regulations
  • Discuss applications for developing technology to improve food safety verification

venue sponsor

We acknowledge that some topics and speakers may be significantly altered or changed due to the government shutdown. This agenda is subject to change.


Industry & Firms

  • +$200 for non-members


  • +$100 for non-members


  • +$100 for non-members


  • +$100 for non-members


  • full-time students only

Are You New to Food Law?

Add the two-day training course, Introduction to Food Law and Regulation, to your schedule to get a comprehensive overview of the laws and regulations affecting the food industry.

To ensure that FDLI is able to provide you with a seat, materials, and meals, please register for programs at least 48 hours in advance. While onsite registration is available on a “space-available” basis; late registrants are not guaranteed materials or meals.

You can transfer your registration to another person at your organization for no cost by notifying us of the change. If you notify FDLI in writing at least five business days prior to the meeting, you can cancel your registration for a full refund (less a $75 fee). Refunds will be applied against the original form of payment.  

Our event policies are listed here. If you should have any further questions, please contact us at [email protected] or 800-956-6293.


Proposal Submission Timeline

  • September 25: Call for Proposals opens.
  • October 25 : Call for Proposals closes.
  • January : Those who submitted proposals will be notified of their submission’s status.


  • Speaking opportunities are generally reserved for FDLI members.
  • Please keep in mind all submissions will be treated as recommendations, and proposals may be modified or combined to best suit the needs of our audience.
  • All submissions must be received through the submission portal.


Sponsorship opportunities are available. Please let us know if you would like more information


We acknowledge that some topics and speakers may be significantly altered or changed due to the government shutdown.

This agenda is subject to change.


Wednesday, March 20

5:00 – 6:00 PM
Hosted by Squire Patton Boggs

Thursday, March 21

8:15 – 8:55 AM
Registration and Continental Breakfast

8:55 – 9:00 AM
FDLI Welcome
Amy Comstock Rick, President & CEO, FDLI

9:00 – 9:45 AM
Keynote Address
Frank Yiannas
, Deputy Commissioner for Food Policy and Response, Office of the Commissioner, FDA
Introduced by John M. Packman, Of Counsel, DLA Piper LLP (US)

9:45 – 10:00 AM
Coffee and Networking Break

10:00 – 11:00 AM
Inspections, Warning Letters, and Compliance: FSMA Begins to Take Hold
Is FDA moving from education to enforcement? Recently issued warning letters show that FDA is beginning to actively enforce the new Preventive Controls rule. On the other hand, FDA continues to educate companies about its new Intentional Adulteration rule. During this panel, speakers will focus on FDA’s current approach to the enforcement of FSMA requirements, as well as discuss inspection trends, warning letters, and other areas on which companies should focus to ensure compliance.

Steve H. Armstrong, Independent Advisor, Food Law & Regulation, EAS Consulting Group, LLC
Meredith Q. Olearchik, Vice President and General Counsel, Intellectual Property, Marketing and Food Law, Campbell Soup Company
Moderated by Elizabeth B. Fawell, Partner, Hogan Lovells US LLP

11:00 AM – 12:00 PM
Traditional Meat and Dairy Foods and Innovative Substitutes: Key Regulatory and Enforcement Issues
Learn about labeling issues and compliance challenges for alternative foods like lab-grown meat and plant-based “dairy”. Panelists will discuss any insights learned once the comment period on the use of names of dairy foods in labeling plant-based products closes at the end of January. Further, speakers will discuss recent developments affecting products in these categories and regulatory risks faced by industry for these and future products in development.

Elan Abrell, Senior Regulatory Specialist, The Good Food Institute
Eitan N. Bernstein, Associate, Lathan & Watkins LLP
Moderated by Sarah Roller, Partner, Kelley Drye & Warren LLP


12:00 – 1:15 PM
Luncheon with Guest Speaker

1:15 – 2:00 PM
Supply Chain Verification Challenges and Realities
This panel will take a practical look at supply chain verification in light of the realities of the food supply chain and how companies are working to comply with FDA’s supply chain verification requirements under FSMA. Panelists will discuss the challenges and hurdles with effective supplier verification and compliance with FDA’s rules.

Jenna Robeson, Senior Director, Regulatory Affairs & Compliance, Plated
Moderated by
Kelly Laudon, Of Counsel, Jones Day

2:00 – 2:45 PM
Managing Through and Learning From Recalls
This panel will focus on practical tools for managing a recall, from the test result or consumer complaint to the close out. While an outbreak of a foodborne illness can lead to a high-profile, national recall, many situations are simply not as clear-cut. This panel will discuss how a firm should define and control the scope of a “voluntary” recall initiated as a result of mislabeling, insanitary conditions, and other frequently occurring issues. When do you know whether to conduct a recall? The panel will use the recent romaine lettuce outbreaks as a lens through which to discuss recall management and avoidance.

Joseph A. Levitt, Partner, Hogan Lovells US LLP
Moderated by
Smitha G. Stansbury, Partner, FDA & Life Sciences Practice, King & Spalding LLP

2:45 – 3:00 PM
Networking Break

3:00 – 3:45 PM
Criminal Enforcement
Some companies have may have a perception that they don’t have to worry about criminal enforcement in the food sphere—this panel will dispel that myth. Speakers will include a review of recent prosecutions and give practical advice for clients facing or hoping not to face that reality.

Howard R. Sklamberg, Partner, Akin Gump Strauss Hauer & Feld LLP
Jack Wenik, Member of the Firm, Epstein Becker & Green, PC

3:45 – 4:45 PM
Class Actions: The Next Phase
During this panel, speakers will address current and recent class actions in the food space. Considering the increasingly active role of class action suits as a form of enforcement, what are best practices to protect your client? What should be your first priorities when the complaint is served? What are some of the key issues to consider in connection with relabeling and settlement?

Anthony Anscombe, Partner, Steptoe & Johnson LLP
Marisol C. Mork
, Partner, Squire Patton Boggs LLP

4:45 PM
Closing Remarks and Adjournment

Planning Committee

Committee Chair

John M. Packman, Of Counsel, DLA Piper LLP (US)

Committee Members

Steve H. Armstrong, Independent Advisor, Food Law & Regulation, EAS Consulting Group, LLC
Elizabeth Barr Fawell, Partner, Hogan Lovells US LLP
Trevor Findley, Deputy Director, Food Disclosure and Labeling, USDA
Megan L. Olsen, Assistant General Counsel, Council for Responsible Nutrition
Jenna Robeson, Senior Director, Regulatory Affairs & Compliance, Plated
Sarah Roller, Partner – Chair Food & Drug Law Practice, Kelley Drye & Warren LLP
Jason W. Sapsin, Counsel, Faegre Baker Daniels LLP
Smitha G. Stansbury, Partner, FDA & Life Sciences Practice, King & Spalding LLP

Continuing Legal Education

FDLI applies for CLE credits in Ohio, Pennsylvania, and Virginia. These CLE approvals may also be honored by other states. The CLE credits will be posted as they are granted and you can request to be notified when approval is received.


Location and Overnight Accommodations

Conference Location

Squire Patton Boggs
2550 M St. NW
Washington, DC 20037

Parking and Public Transportation

Squire Patton Boggs is located in Washington DC’s West End, with easy access to major commuting routes and public transportation. For information about Metro locations and parking in the vicinity, please see Available Parking and Metro Information.


Overnight Accommodations

A block of rooms has been reserved for course attendees at the Westin Georgetown Hotel.   The Westin Georgetown is a short walk from the course location.  Reservations can be made online and must be received by Monday, February 18 to obtain the $279 group rate.  After this date, rooms will be subject to prevailing rates and availability.