Committee on the Public Health Effectiveness of the FDA 510(k) Clearance Process – författare

Visar alla böcker från författaren Committee on the Public Health Effectiveness of the FDA 510(k) Clearance Process. Handla med fri frakt och snabb leverans.

8 produkter

1. 

   Public Health Effectiveness of the FDA 510(k) Clearance Process

   Balancing Patient Safety and Innovation: Workshop Report

   Av Institute of Medicine, Board on Population Health and Public Health Practice m. fl.

   Häftad, 2010

   751 kr

   Lägg i varukorg

   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 …

2. 

   Public Health Effectiveness of the FDA 510(k) Clearance Process

   Balancing Patient Safety and Innovation: Workshop Report

   Av Committee on the Public Health Effectiveness of the FDA 510(k) Clearance Process, Board on Population Health and Public Health Practice m. fl.

   E-bok, 2010

   473 kr

   Lägg i varukorg

   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 …

3. 

   Public Health Effectiveness of the FDA 510(k) Clearance Process

   Measuring Postmarket Performance and Other Select Topics: Workshop Report

   Av Committee on the Public Health Effectiveness of the FDA 510(k) Clearance Process, Board on Population Health and Public Health Practice m. fl.

   E-bok, 2011

   616 kr

   Lägg i varukorg

   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 requires a manufacturer of medical devices to notify FDA of its intent to market a medical device …

4. 

   Public Health Effectiveness of the FDA 510(k) Clearance Process

   Balancing Patient Safety and Innovation: Workshop Report

   Av Committee on the Public Health Effectiveness of the FDA 510(k) Clearance Process, Board on Population Health and Public Health Practice m. fl.

   E-bok, 2010

   658 kr

   Lägg i varukorg

   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 …

5. 

   Medical Devices and the Public's Health

   The FDA 510(k) Clearance Process at 35 Years

   Av Committee on the Public Health Effectiveness of the FDA 510(k) Clearance Process, Board on Population Health and Public Health Practice m. fl.

   E-bok, 2011

   892 kr

   Lägg i varukorg

   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 organizations have expressed concern that the 510(k) process is neither making safe and effective devices …

6. 

   Medical Devices and the Public's Health

   The FDA 510(k) Clearance Process at 35 Years

   Av Committee on the Public Health Effectiveness of the FDA 510(k) Clearance Process, Board on Population Health and Public Health Practice m. fl.

   E-bok, 2011

   981 kr

   Lägg i varukorg

   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 organizations have expressed concern that the 510(k) process is neither making safe and effective devices …

7. 

   Public Health Effectiveness of the FDA 510(k) Clearance Process

   Measuring Postmarket Performance and Other Select Topics: Workshop Report

   Av Committee on the Public Health Effectiveness of the FDA 510(k) Clearance Process, Board on Population Health and Public Health Practice m. fl.

   E-bok, 2011

   642 kr

   Lägg i varukorg

   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 requires a manufacturer of medical devices to notify FDA of its intent to market a medical device …

8. 

   Medical Devices and the Public's Health

   The FDA 510(k) Clearance Process at 35 Years

   Av Institute of Medicine, Board on Population Health and Public Health Practice m. fl.

   Häftad, 2011

   558 kr

   Tillfälligt slut

   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 organizations have expressed concern that the 510(k) process is neither making safe and effective devices …