Updates for 2021
FDLI remains committed to providing high-quality educational programs while keeping our members and event attendees safe during the current pandemic. With this in mind, we are excited to announce that the 2021 Enforcement, Litigation, and Compliance Conference will be a virtual event. Please know we are actively exploring options to ensure an engaging and enjoyable experience. Be sure to check the conference website regularly for additional announcements and updates.
The annual Enforcement, Litigation, and Compliance Conference brings together industry, regulators, attorneys, litigators, academics, and consultants to discuss trends and issues in enforcement and compliance, the latest developments in both civil and criminal litigation, and recent cases and settlements. This year’s conference will be a virtual event, offering an opportunity to hear from and interact with top officials from FDA, DOJ, FTC, and other government agencies. As we move out of the COVID-19 pandemic, come hear from your peers about how they are staying compliance and inspection ready as FDA ramps back up inspections, what companies need to do to plan for and manage enforcement risk, trends in criminal and civil litigation, and government priorities for the new year.
Conference Highlights:
- Hear about top issues, priorities, and goals for 2022 directly from ORA and FDA’s Center Compliance Directors
- Gain practical tips and best practices on preparing for and managing enforcement and compliance risk in a post-COVID era
- Learn about trends in government and private litigation, and what happens post-emergency and enforcement discretion periods
Register
Industry & Firms
- +$200 for non-members
Non-Profit
- +$100 for non-members
Government
- +$100 for non-members
Academic
- +$100 for non-members
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Sponsors
Sponsorship opportunities are available. Please let us know if you would like more information.
Call for Proposals
FDLI and the Conference Planning Committee thanks those who participated in the Call for Proposals this summer. The input received from industry stakeholders helps us plan a timely program. If you submitted a proposal, you will be notified of the status of your proposal in September.
Planning Committee
Chair
Bob Rhoades, Validant
Committee Members
Hannah R. Bornstein, Nixon Peabody LLP
Adrienne Franco Busby, Faegre Drinker Biddle & Reath LLP
Philip Crooker, Parexel International Corporation
Maya Florence, Skadden, Arps, Slate, Meagher & Flom LLP
Elizabeth A. Gallenagh, Healthcare Distribution Alliance (HDA)
William Gould, Holland & Knight LLP
Dennis C. Gucciardo, Morgan, Lewis & Bockius LLP
Stephanie M. Haggerty, Pfizer, Inc.
Bryan M. Haynes, Troutman Pepper Hamilton Sanders LLP
Winston S. Kirton, Winston & Strawn LLP
Pete Leininger, King & Spalding LLP
Donnelly McDowell, Kelley Drye & Warren LLP
Anne K. Miller, Medtronic
John A. Murphy III, Biotechnology Innovation Organization
Ann Oxenham, OC, FDA
Allen Sayler, EAS Consulting Group
Lora J. Spencer, Reed Smith LLP
William Stellmach, Willkie Farr & Gallagher LLP
Frances Zipp, Lachman Consultants