This webinar was recorded on Tuesday, 23rd April 2024.

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

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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

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Moderator + Hosts:

• Megan Nacar, VP of Commercial, DeciBio Consulting
• Stephane Budel, PhD, Partner, DeciBio Consulting
• Maximilian Schmid, MD, Senior Advisor, Independent Consultant

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View the webinar recording and slides below:

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