Paperback (04 Oct 2010)
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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."--.
| ISBN: | 9780309158497 |
| Publisher: | National Academies Press |
| Imprint: | National Academies Press |
| Pub date: | 04 Oct 2010 |
| DEWEY: | 610 |
| DEWEY edition: | 22 |
| Language: | English |
| Weight: | 249g |
| Height: | 229mm |
| Width: | 152mm |
| Spine width: | 8mm |
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