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Code of Federal Regulations, Title 21, Food and Drugs, PT. 1-99, 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: 0160938090     ISBN-13: 9780160938092
Publisher: Government Printing Office
OUR PRICE:   $42.75  
Product Type: Paperback
Published: July 2017
Qty:
Temporarily out of stock - Will ship within 2 to 5 weeks
Additional Information
BISAC Categories:
- Law | Administrative Law & Regulatory Practice
- Medical | Pharmacology
- Medical | Allied Health Services - Medical Technology
Physical Information: 1" H x 5.75" W x 9.13" (1.43 lbs) 594 pages
 
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 currently the Official U.S. Federal Government edition of this product.

Title 21 CFR, Parts 1-99, includes rules, regulations, procedures and administrative procedures associated with the Food and Drug Administration and the Department of Health and Human Services (administrative practices, electronic records, public hearings), environmental impact considerations, pharmaceutical good manufacturing practice reports, medical device quality system audit reports/device product evaluation reports (in the United States and European community), protection of human subjects, financial disclosure by clinical investigators, good laboratory practice, patent term restoration, color additives, and more..

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