Why Attend?

Agenda
CLE

This year’s conference is going virtual! An entirely virtual format will enable innovative learning opportunities, increased schedule flexibility, and a new level of interaction between regulatory practitioners, industry experts, and government officials. Speakers will analyze the latest commercial issues related to advertising and promotion of human and animal drugs, medical devices, and biologics.

Practical Takeaways: Sessions will explore updated government agency enforcement trends, competitor actions, the current state of unapproved use promotion, patient engagement, management of risk in the current climate, and the increasing challenges of various direct-to-consumer marketing platforms.

Government Speakers: Representatives from various FDA Centers, the Federal Trade Commission, the Department of Health and Human Services Inspector General, and the Department of Justice will provide the latest information on policy, enforcement, and future initiatives.

Peer Interaction: The conference will prioritize virtual learning, engagement, and networking with fellow legal, regulatory, and marketing experts.

Register

Industry & Firms

$1499
  • +$400 for non-members

Non-Profit

$799
  • +$100 for non-members

Government

$799
  • +$100 for non-members

Academic

$799
  • +$100 for non-members

Student

$99
  • full-time students only

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On-Demand Access Available to Registrants

As a registrant, you will receive access to the recorded live sessions of the conference through November 27. Use this access to revisit engaging sessions, or to catch the sessions you weren’t able to attend in real time.

Are You New to Advertising and Promotion?

Add the training course, Introduction to Advertising and Promotion for Medical Products, to your conference registration to gain a comprehensive overview of the laws and regulations affecting the medical products industries. Register for both the conference and course to save $100 off the combined fees.

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.

Sponsors

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

 

Gold Sponsor

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Gold Sponsor

 

Silver Sponsor

 

Silver Sponsor

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Silver Sponsor

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Call for Proposals

FDLI and the Conference Planning Committee thanks those who participated in the Call for Proposals. The input received from industry stakeholders helps us plan a timely program. 

 

 

Planning Committee

Fadwa Almanakly, Bayer Healthcare Pharmaceuticals
Heather Banuelos, (Co-Chair), King & Spalding LLP 
Madhavi Bellamkonda, Abbott Vascular
Blythe Buchanan, Biogen, Inc.
Rebecca Burnett, Framework Solutions
Dale Cooke, PhillyCooke Consulting
Mary Ellen Dronitsky, Arena Pharmaceuticals
Virginia Foley, Opus Regulatory Inc
Mark Garsombke, Hall, Render, Killian, Heath & Lyman P.C.
Bryant M. Godfrey, Arnold & Porter LLP
Mark C. Levy, Eckert Seamans Cherin & Mellott, LLC
Lauren A. Miller, Otsuka America Pharmaceutical, Inc.
Cassie Scherer, Medtronic
Dolores M. Shank-Samiec, (Co-Chair), Merck & Co., Inc. 
Michael Francis Smith, Michael F. Smith Law, PLLC