The FDA and Worldwide Quality System Requirements Guidebook for Medical Devices (Hardcover, 2nd ed.)

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.

General

Imprint:	ASQ Quality Press
Country of origin:	United States
Release date:	June 2008
Authors:	Amiram Daniel
Dimensions:	234 x 157 x 25mm (L x W x T)
Format:	Hardcover - Sewn / Cloth over boards
Pages:	304
Edition:	2nd ed.
ISBN-13:	978-0-87389-740-2
Categories:	Books > Law > Laws of other jurisdictions & general law > Constitutional & administrative law > General Promotions
LSN:	0-87389-740-4
Barcode:	9780873897402

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