When: 

Tuesday, April 23, 2024

09:00 AM PT / 12:00 PM ET / 04:00 PM UK

What to expect:

Join us for a digital executive roundtable discussion of DeciBio's white paper "Regulatory Reckoning: Navigating the FDA's Laboratory Developed Tests Regulation". Free download available here.

Meet the authors of the white paper, DeciBio's co-founding partner, Dr. Stephane Budel, and Senior Advisor, Dr. Maximillian Schmid as they moderate a discussion with different stakeholders across the ecosystem.

Our invited stakeholders bring a diverse perspective on the matter:

• Legal

• FDA Strategy

• Reimbursement

• Validation

Speakers:

Shannon Bennett - Director of Regulatory Affairs, Mayo Clinic 

Sarah Clancey Overton - Senior Director of Revenue Cycle Management, Velsera

Jon Harol - President & Founder, Lighthouse Lab Services

Bruce Quinn, MD, PhD - Principal, Bruce Quinn Associates LLC

Paul Gadiock, JD - Partner, McDermott Will & Emery

Mike Ryan, JD - Partner, McDermott Will & Emery