Public health effectiveness of the fda 510(k) clearance process: balancing patient safety and innovation: workshop report
Auteur :
Institute of Medicine / Board on Population Health and Public Health Practice / Committee on the Public Health Effectiveness of the FDA 510(k) Clearance Process
Éditeur :
National Academies Press
ISBN :
9780309158497
Date de publication :
4 oct. 2010
Dimensions :
22,9 x 15,2 cm
Langue :
Anglais
Pays d'origine :
USA
The Food and Drug Administration (FDA) is responsible for assuring that medical devices are safe and effective before they go on the market. As part of its assessment of FDA's premarket clearance process for medical devices, the IOM held a workshop June 14-15 to discuss how to best balance patient safety and technological innovation.