Public Health Effectiveness of the FDA 510(k) Clearance Process - Institute of Medicine, Board on Population Health and Public Health Practice, Committee on the Publi

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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.

Titel

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

Untertitel

Balancing Patient Safety and Innovation: Workshop Report

Autor

Institute of Medicine

Board on Population Health and Public Health Practice

Committee on the Publi

Editor

Theresa Wizemann

EAN

9780309162906