Public Health Effectiveness of the FDA 510(k) Clearance Process
Balancing Patient Safety and Innovation: Workshop Report
Herausgeber: Wizemann, Theresa
Versandkostenfrei!
Versandfertig in über 4 Wochen
45,99 €
inkl. MwSt.
PAYBACK Punkte
23 °P sammeln!
"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. This document summarizes the workshop."--
Andere Kunden interessierten sich für
