Code of Federal Regulations, Title 21, Food and Drugs, Pt. 800-1299, Revised as of April 1, 2018 Revised Edition Contributor(s): Office of the Federal Register (U S ) (Editor), National Archives and Records Administra (Editor) |
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ISBN: 0160945461 ISBN-13: 9780160945465 Publisher: Government Printing Office OUR PRICE: $62.70 Product Type: Paperback Published: August 2018 |
Additional Information |
BISAC Categories: - Law | Administrative Law & Regulatory Practice - Medical | Allied Health Services - Medical Technology - Medical | Physician & Patient |
Physical Information: 945 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 updated 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... |