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Bethesda North Marriott Hotel and Conference Center

Feb 02, 2026 10:00 AM - Feb 04, 2026 12:45 PM

5701 Marinelli Road, North Bethesda, MD 20852

Regulatory Submissions, Information, and Document Management Forum

Don't miss the latest trends, innovations, and best practices in regulatory submissions, information, and document management (RSIDM)!

Session 1: Opening Plenary - Achieving Regulatory Excellence: A Sponsor and Patient Perspective

Session Chair(s)

Jared  Lantzy, PMP

Jared Lantzy, PMP

Executive Director, Global Regulatory Affairs Operations, Novavax, Inc., United States

Noelia  Plaza

Noelia Plaza

Director of Process Excellence & Analytics, Daiichi Sankyo, United States

Join a facilitated fireside chat where we will hear both a sponsor and patient perspective of what Regulatory Excellence means and how we achieve it. Our panelists will discuss how Regulatory Excellence has evolved in the digital age and how we expect it will change given ongoing transformations. In addition, we will be reminded of the patient impact of our work and how our day-to-day work is crucial in ensuring that life-saving products reach those that need them.

Henrietta N. Ukwu, Novavax Inc

Carlos Garner, Eli Lilly and Company

Jamey Ann Galione, Bristol-Myers Squibb Company

Speaker(s)

Henrietta N. Ukwu, MD, FACP

Speaker

Henrietta N. Ukwu, MD, FACP

Executive Vice President and Chief Regulatory Officer, Novavax, United States

Carlos  Garner, PhD, MSc

Speaker

Carlos Garner, PhD, MSc

Senior Vice-President Global Regulatory Affairs and Head, Lilly Regenerative Med, Eli Lilly and Company, United States

Jamey  Galione

Speaker

Jamey Galione

Director, CMC Submission Management, Bristol Myers Squibb, United States

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