NSPE Member Advises FDA on External Defibrillator Improvement

Wednesday, December 15, 2010

NSPE Senior Manager of Government Relations Sarah Ogden and NSPE member Robert Cargill, Ph.D., P.E., attended a Food and Drug Administration External Defibrillator Improvement Initiative workshop. Cargill participated in a panel discussion on engineering design practices that could improve the next generation of devices.

The Food and Drug Administration's Center for Devices and Radiological Health has launched the External Defibrillator Improvement Initiative to encourage innovation in and improve the safety and effectiveness of the next generation of external defibrillators. While FDA urges consumers to continue using current external defibrillators, the agency hopes to improve design and manufacturing practices to enhance future devices and reduce instances of failure.