Three representatives of the Food and Drug Administration will be on hand Monday evening to discuss regulatory updates at a panel discussion sponsored by the North Carolina Medical Device Association.

The discussion begins at 5 PM followed by a reception at the North Carolina Biotechnology Center.

Panelists include:

  • Patricia Love, Associate Director, FDA Office of Combination Products

  • Heather Rosecrans, Director 510(k) Staff, FDA Center for Devices & Radiological Health

  • Les Weinstein, Ombudsman, FDA Center for Devices & Radiological Health

  • Tammy Carrea, Director, Regulatory Affairs, Sicel Technologies

  • Dan Pelak (Moderator), President & CEO, Closure Medical
  • For details, see: www.ncmedicaldevice.org/Events.html