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

- Balancing Patient Safety and Innovation: Workshop Report

av Institute of Medicine
Public Health Effectiveness of the FDA 510(k) Clearance Process av Institute of Medicine
Om 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 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."--

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  • Språk:
  • Engelska
  • ISBN:
  • 9780309158497
  • Format:
  • Häftad
  • Sidor:
  • 140
  • Utgiven:
  • 4 November 2010
  • Mått:
  • 152x229x8 mm.
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Leveranstid: 2-4 veckor
Förväntad leverans: 24 Oktober 2024

Om Institute of Medicine

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Beskrivning av 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 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."--

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