Code of Federal Regulations Title 21, Food and Drugs, Parts 600-799, 2022
Title | Code of Federal Regulations Title 21, Food and Drugs, Parts 600-799, 2022 PDF eBook |
Author | National Archives and Records Administration |
Publisher | |
Pages | 0 |
Release | 2022-04 |
Genre | |
ISBN | 9781638263166 |
Code of Federal Regulations, Title 21 Food and Drugs 600 - 799, 2022
Title | Code of Federal Regulations, Title 21 Food and Drugs 600 - 799, 2022 PDF eBook |
Author | Office Of The Federal Register (U.S.) |
Publisher | Code of Federal Regulations, Title 21 Food and Drugs |
Pages | 0 |
Release | 2023-03-31 |
Genre | |
ISBN | 9781636711935 |
Title 21 presents regulations promulgated by the Food and Drug Administration, the Drug Enforcement Administration, and the Office of the National Drug Control Agency in the area of food and drugs. These regulations encompass food and drugs for human and animal use, biologics, cosmetics, medical devices, radiological health, and controlled substances. Additions and revisions to this section of the code are posted annually by April. Publication follows within six months.
Code of Federal Regulations, Title 21
Title | Code of Federal Regulations, Title 21 PDF eBook |
Author | National Archives and Records Administra |
Publisher | |
Pages | 0 |
Release | 2010-07-16 |
Genre | |
ISBN | 9781609460679 |
Title 21 presents regulations promulgated by the Food and Drug Administration, the Drug Enforcement Administration, and the Office of the National Drug Control Agency in the area of food and drugs. These regulations encompass food and drugs for human and animal use, biologics, cosmetics, medical devices, radiological health, and controlled substances. Additions and revisions to this section of the code are posted annually by April. Publication follows within six months.
Code of Federal Regulations, Title 21, Food and Drugs, Pt. 600-799, Revised as of April 1, 2009
Title | Code of Federal Regulations, Title 21, Food and Drugs, Pt. 600-799, Revised as of April 1, 2009 PDF eBook |
Author | |
Publisher | Government Printing Office |
Pages | 220 |
Release | 2009-07-09 |
Genre | Law |
ISBN | 9780160828867 |
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.
Code of Federal Regulations, Title 21, Food and Drugs, Pt. 600-799, Revised as of April 1, 2010
Title | Code of Federal Regulations, Title 21, Food and Drugs, Pt. 600-799, Revised as of April 1, 2010 PDF eBook |
Author | |
Publisher | Government Printing Office |
Pages | 220 |
Release | 2010-06-16 |
Genre | Law |
ISBN | 9780160853838 |
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.
Code of Federal Regulations Title 21, Food and Drugs, Pt. 600 to 799, Revised As of April 1 2017
Title | Code of Federal Regulations Title 21, Food and Drugs, Pt. 600 to 799, Revised As of April 1 2017 PDF eBook |
Author | Office of the Federal Register (US) |
Publisher | Createspace Independent Publishing Platform |
Pages | 210 |
Release | 2017-12-07 |
Genre | |
ISBN | 9781981462605 |
THIS TITLE Title 21-FOOD AND DRUGS is composed of nine volumes. The parts in these volumes are arranged in the following order: Parts 1-99, 100-169, 170-199, 200-299, 300-499, 500-599, 600-799, 800-1299 and 1300-end. The first eight volumes, containing parts 1-1299, comprise Chapter I-Food and Drug Administration, Department of Health and Human Services. The ninth volume, containing part 1300 to end, in-cludes Chapter II-Drug Enforcement Administration, Department of Justice, and Chapter III-Office of National Drug Control Policy. The contents of these vol-umes represent all current regulations codified under this title of the CFR as of April 1, 2017.
Code of Federal Regulations
Title | Code of Federal Regulations PDF eBook |
Author | Aabb |
Publisher | S. Karger AG (Switzerland) |
Pages | 0 |
Release | 2005 |
Genre | |
ISBN | 9783805580427 |
This section of the Code of Federal Regulations codifies the general and permanent rules established by the Food and Drug Administration (FDA) that pertain to whole blood and blood products. This section addresses FDA registration and licensure requirements for establishments, personnel requirements, record keeping, labeling, good manufacturing practice and additional specific requirements for whole blood and blood products.