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Zustand: New. This is a Brand-new US Edition. This Item may be shipped from US or any other country as we have multiple locations worldwide.
Sprache: Englisch
Verlag: Nova Science Publishers, Incorporated, 2012
ISBN 10: 1622570898 ISBN 13: 9781622570898
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Sprache: Englisch
Verlag: Nova Science Publishers, Incorporated, 2012
ISBN 10: 1622570898 ISBN 13: 9781622570898
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Zustand: Used.
Sprache: Englisch
Verlag: Nova Science Publishers Inc, 2012
ISBN 10: 1622570898 ISBN 13: 9781622570898
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HRD. Zustand: New. New Book. Shipped from UK. Established seller since 2000.
Sprache: Englisch
Verlag: Nova Science Publishers Inc, 2012
ISBN 10: 1622570898 ISBN 13: 9781622570898
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EUR 149,91
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In den WarenkorbHRD. Zustand: New. New Book. Shipped from UK. Established seller since 2000.
Sprache: Englisch
Verlag: Nova Science Publishers Inc, 2012
ISBN 10: 1622570898 ISBN 13: 9781622570898
Anbieter: Kennys Bookstore, Olney, MD, USA
Zustand: New. Editor(s): Hill, Matthew W.; Torres, Daniel E. Num Pages: 150 pages, illustrations. BIC Classification: JPP; LNTM2. Category: (G) General (US: Trade). Dimension: 162 x 236 x 17. Weight in Grams: 388. . 2012. 1st Edition. Hardcover. . . . . Books ship from the US and Ireland.
Sprache: Englisch
Verlag: Nova Science Publishers Inc, 2012
ISBN 10: 1622570898 ISBN 13: 9781622570898
Anbieter: moluna, Greven, Deutschland
Zustand: New. KlappentextrnrnThe FDA is responsible for overseeing the safety and effectiveness of medical devices sold in the United States. New devices are generally subject to FDA review via the 510(k) process, which determines if a device is substantially.
Sprache: Englisch
Verlag: Nova Science Publishers Inc Nov 2012, 2012
ISBN 10: 1622570898 ISBN 13: 9781622570898
Anbieter: AHA-BUCH GmbH, Einbeck, Deutschland
Buch. Zustand: Neu. Neuware - The FDA is responsible for overseeing the safety and effectiveness of medical devices sold in the United States. New devices are generally subject to FDA review via the 510(k) process, which determines if a device is substantially equivalent to another legally marketed device, or the more stringent pre-market approval process, which requires evidence providing reasonable assurance that the device is safe and effective. This book examines whether the FDA is sufficiently meeting the performance goals and whether devices are reaching the market in a timely manner.