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Code of Federal Regulations, Title 21, Food and Drugs, PT. 800-1299, Revised as of April 1, 2017 Revised Edition
Contributor(s): Office of the Federal Register (U S ) (Editor), National Archives and Records Administra (Editor)
ISBN: 0160938163     ISBN-13: 9780160938160
Publisher: Government Printing Office
OUR PRICE:   $62.70  
Product Type: Paperback
Published: June 2017
Qty:
Temporarily out of stock - Will ship within 2 to 5 weeks
Additional Information
BISAC Categories:
- Law | Administrative Law & Regulatory Practice
- Medical | Allied Health Services - Medical Technology
- Medical | Physician & Patient
Physical Information: 1.5" H x 5.75" W x 9.13" (2.18 lbs) 899 pages
Themes:
- Sex & Gender - Feminine
- Topical - Health & Fitness
 
Descriptions, Reviews, Etc.
Publisher Description:
The Code of Federal Regulations is a codification of the general and permanent rules published in the Federal Register by the Executive departments and agencies of the United States Federal Government. This print ISBN is the official U.S. Federal Government edition.

Title 21 CFR, Parts 800-1299, includes rules, regulations, procedures and administrative procedures associated with the Food and Drug Administration and Department of Health and Human Services (medical devices), medical device quality system regulation, postmarket surveillance, unique device identification, medical device classification procedures, mammography, the Mammography Quality Standards Act, radiological health, tobacco products, the Federal Import Milk Act, the Federal Caustic Poison Act, control of communicable diseases, human tissue intended for transplantation, and more...

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