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Medical Devices Law and Regulation Answer Book
Language: en
Pages: 0
Authors: Suzan Onel
Categories: Medical instruments and apparatus
Type: BOOK - Published: 2022 - Publisher:

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Medical Devices Law and Regulation Answer Book
Language: en
Pages: 1220
Authors: Suzan Onel
Categories: Law
Type: BOOK - Published: 2018-11-06 - Publisher:

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In Medical Devices Law and Regulation Answer Book, more than thirty contributors from various law and consulting firms share their expertise regarding the laws
Public Health Effectiveness of the FDA 510(k) Clearance Process
Language: en
Pages: 141
Authors: Institute of Medicine
Categories: Medical
Type: BOOK - Published: 2010-10-04 - Publisher: National Academies Press

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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 asse
Medical Devices and the Public's Health
Language: en
Pages: 318
Authors: Institute of Medicine
Categories: Medical
Type: BOOK - Published: 2011-11-25 - Publisher: National Academies Press

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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
Medical Devices Law and Regulation Answer
Language: en
Pages: 960
Authors: Karen Becker
Categories: Law
Type: BOOK - Published: 2011 - Publisher: Practising Law Inst

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