| Code of Federal Regulations, Title 21, Food and Drugs, PT. 800-1299, Revised as of April 1, 2016 Contributor(s): Office of the Federal Register (U S ) (Editor), National Archives and Records Administra (Editor) |
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ISBN: 0160932769 ISBN-13: 9780160932762 Publisher: Government Printing Office OUR PRICE: $62.70 Product Type: Paperback Published: July 2016 |
| Additional Information |
| BISAC Categories: - Law | Administrative Law & Regulatory Practice - Medical | Allied Health Services - Medical Technology - Business & Economics | Industries - Manufacturing |
| Physical Information: 1.8" H x 6" W x 9" (2.60 lbs) 868 pages |
| Descriptions, Reviews, Etc. |
| Publisher Description: This print ISBN is the U.S. Federal Government Official edition of this title. 21 CFR Parts 800 to 1299 covers the U. S. Food and Drug Administration within the U.S. Department of Health and Human Services. Within this volume, you will find rules, procedures, and regulations pertaining to medical devices, such as cardiovascular devices, dentistry devices, orthopedic, gastroenterology-urology, in vitro, anestheology, and more. Plus, you will find rules, procedures, and regulations relating to mammography quality standards, radiological health, tobacco products, cigarette package advertising warnings, cigarettes and smokeless tobacco, human tissue intended for transplantation, and more. Audiences: medical device producers and marketers, medical practitioners, tobacco proudcers andmarketers, human health researchers and practioners. Healthcare device manufacturers, hosptital radiological and other medical technicians and departments, physicians, nurses, out-patient clinics' personnel, and healthcare policy advocates, tobacco producers and advertisers/marketers as well as human health researchers and practitionersmay be interested in this volume." |