$ 194.450
Autor( a ): AA. VV.
Editorial: National Academies Press
Año de Edición: 2010-10-04
Formato: Libro Impreso Bajo Demanda
100 disponibles
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.
| Peso | 0,215 kg |
|---|---|
| Dimensiones | 0,793 × 15,2 × 22,9 cm |
| ISBN | 9780309158497 |
| Autor | AA. VV. |
| Editorial | National Academies Press |
| Año De Edición | 2010-10-04 |
| Número De Páginas | 140 |
| País | Estados Unidos de América (EE.UU.) |
| Formato | Libro Impreso Bajo Demanda |
| Terminado | Tapa Blanda |
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