Release Date: 01 October, 2002
Hardcover
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From Book News, Inc. Approaching design control as a mandated regulation for the medical device industry in the United States, consultants Teixera and Bradley offers advice on harmonizing product development models with the requirements of the U.S. Food and Drug Administration (FDA). They discuss the development of products in a step-by-step fashion, moving from design and development planning; through review, verification, and validation; to dealing with an FDA audit.Book News, Inc.®, Portland, OR Rating
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