The FDA and Worldwide Quality System Requirements Guidebook for Medical Devices

Quality Press
Free sample

How have recent changes in domestic and international regulations affected quality management in the development and marketing of medical devices in the US and abroad? Consultants Daniel and Kimmelman take a close look at the Quality System Regulation (QsReg), the ISO 13485: 2003 standard and the ISO/TR 14969: 2004 guidance document as well as a number of US Food and Drug Administration (FDA) and Global Harmonization Task Force (GHTF) guidance documents. The authors provide extensive commentary and notes an update their material to include such topics as the incorporation of principles of risk management into the medical device organizations' quality management systems (QMSs) and considerations of combination products. Daniel and Kimmelman include full coverage of the QSReg requirements, descriptions of comparable requirements in the ISO documents, excerpts of the FDA's responses to the QSReg preamble and excerpts from FDA guidance documents related to QMSs.
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Additional Information

Publisher
Quality Press
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Published on
Jan 1, 2008
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Pages
304
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ISBN
9780873897402
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Language
English
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Genres
Law / Medical Law & Legislation
Medical / Instruments & Supplies
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Content protection
This content is DRM free.
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Available on Android devices
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