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
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
Moderator + Hosts:
- Megan Nacar, VP of Commercial, DeciBio Consulting
- Stephane Budel, PhD, Partner, DeciBio Consulting
- Maximilian Schmid, MD, Senior Advisor, Independent Consultant
View the webinar recording and slides below:
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