Autor: Committee on the Public Health Effectiveness of the FDA 510(k) Clearance Process

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6 Ebooki wg Committee on the Public Health Effectiveness of the FDA 510(k) Clearance Process

Board on Population Health and Public Health Practice & Committee on the Public Health Effectiveness of the FDA 510(k) Clearance Process: Public Health Effectiveness of the FDA 510(k) Clearance Process
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 pro …
PDF
Angielski
DRM
€34.15
Board on Population Health and Public Health Practice & Committee on the Public Health Effectiveness of the FDA 510(k) Clearance Process: Public Health Effectiveness of the FDA 510(k) Clearance Process
The Food and Drug Administration (FDA) is responsible for ensuring that medical devices are safe and effective before they go on the market. Section 510(k) of the Federal Food, Drug, and Cosmetic Act …
PDF
Angielski
DRM
€43.99
Board on Population Health and Public Health Practice & Committee on the Public Health Effectiveness of the FDA 510(k) Clearance Process: Public Health Effectiveness of the FDA 510(k) Clearance Process
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 pro …
EPUB
Angielski
DRM
€48.89
Board on Population Health and Public Health Practice & Committee on the Public Health Effectiveness of the FDA 510(k) Clearance Process: Medical Devices and the Public’s Health
Medical devices that are deemed to have a moderate risk to patients generally cannot go on the market until they are cleared through the FDA 510(k) process. In recent years, individuals and organizat …
PDF
Angielski
DRM
€63.98
Board on Population Health and Public Health Practice & Committee on the Public Health Effectiveness of the FDA 510(k) Clearance Process: Medical Devices and the Public’s Health
Medical devices that are deemed to have a moderate risk to patients generally cannot go on the market until they are cleared through the FDA 510(k) process. In recent years, individuals and organizat …
EPUB
Angielski
DRM
€70.62
Board on Population Health and Public Health Practice & Committee on the Public Health Effectiveness of the FDA 510(k) Clearance Process: Public Health Effectiveness of the FDA 510(k) Clearance Process
The Food and Drug Administration (FDA) is responsible for ensuring that medical devices are safe and effective before they go on the market. Section 510(k) of the Federal Food, Drug, and Cosmetic Act …
EPUB
Angielski
DRM
€46.11