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Provides a general description in plain language of medical device regulation for those who operate in the regulated community company executives, healthcare professionals, medical researchers, and biomedical engineers, among others. The volume describes what the FDA generally would like manufacturers to do, as explained in various laws, regulations, guidances, and manuals. The first chapter presents a history of medical device regulation. The following chapters describe the current state of the law as of September 1, 1994. The final chapter projects the future of device regulation. Annotation copyright Book News, Inc. Portland, Or.
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Book Description Interpharm Pr, 1995. Hardcover. Condition: Used: Good. Seller Inventory # SONG0935184791