Health technology has gained a tremendous amount of momentum and attracted large sums of money from venture capital investors, but founders of health startups must be much more attentive to government regulation than many other sectors. Certain segments of the health market, such as devices being used to diagnose or treat medical conditions, fall under FDA jurisdiction for a variety of premarket and postmarket requirements and clinical trials. Digital health companies may face similarly complex regulatory scrutiny. Join us for a panel to learn about the regulatory environment for health startups. Panelists will also advise founders on how to create a robust IP strategy to build a moat around your startup.
Benjamin Glenn, Partner at Shay Glenn LLP
Jim Swick, Principal at Swick Consulting
Christi Campbell, Partner at Duane Morris
Steven S. Brooks, Principal at Brooks Medtech LLC
Kyle Vos Strache, Member at Cozen O’Connor
Moderator: Dr. Phil Christian, Managing Director of the Dreamit Health Program