A full-day event featuring government and industry experts addressing global regulatory challenges facing life science companies in biotech, pharma, devices, and emerging technologies.
Morning Session: Regulatory Pathway Basics of Drugs, Devices, and Other Regulated Products
Keynote Lunch Speaker: “What Am I?” How To Determine and Get FDA Agreement On Your Product Classification
Afternoon Session: Emerging Technologies (Breakthrough Devices, SWaMD, Stem Cell Tx)
Afternoon “Disaster Panel”: What Happens If a Company Decides to Take a Shortcut or Deviate From Regulations?
Continental breakfast, lunch, and refreshments included.