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Title 21. Displaying title 21, up to date as of 5/10/2024. Title 21 was last amended 5/06/2024. view historical versions. There have been changes in the last two weeks to Title 21. view change. eCFR Content.
- Subchapter H
Subchapter H - eCFR :: Title 21 of the CFR -- Food and Drugs
- 21 CFR Part 11
21 CFR Part 11 - eCFR :: Title 21 of the CFR -- Food and...
- Chapter II
Chapter II - eCFR :: Title 21 of the CFR -- Food and Drugs
- Subchapter B
Subchapter B - eCFR :: Title 21 of the CFR -- Food and Drugs
- Subchapter D
Subchapter D - eCFR :: Title 21 of the CFR -- Food and Drugs
- OTC
OTC - eCFR :: Title 21 of the CFR -- Food and Drugs
- Importation and Production Quotas for Ephedrine, Pseudoephedrine, and Phenylpropanolamine
Importation and Production Quotas for Ephedrine,...
- Subchapter I
Subchapter I - eCFR :: Title 21 of the CFR -- Food and Drugs
- Miscellaneous
Miscellaneous - eCFR :: Title 21 of the CFR -- Food and...
- Subchapter H
Dec 22, 2023 · For the most up-to-date version of CFR Title 21, go to the Electronic Code of Federal Regulations (eCFR). This database includes a codification of the general and permanent rules...
CFR 21 was downloaded from the files of the Government Printing Office (GPO) and contains the most recent revision. The CFR at GPO, both current and historical, can also be searched directly...
The full text of the Code of Federal Regulations, the LSA (List of CFR Sections Affected), The United States Government Manual, the Federal Register, Public Laws, Public Papers of the Presidents of the United States, Compilation of Presi-
Food and Drugs--Volume 1. 21:1.0.1. CHAPTER I - FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES.
Electronic Code of Federal Regulations (e-CFR): Title 21—Food and Drugs. CFR. prev | next. CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (Subchapters A - L) CHAPTER II—DRUG ENFORCEMENT ADMINISTRATION, DEPARTMENT OF JUSTICE (Parts 1300 - 1322-1399) CHAPTER III—OFFICE OF NATIONAL DRUG CONTROL POLICY ...
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Dec 22, 2023 · (a) The regulations in this part contain the minimum current good manufacturing practice for preparation of drug products (excluding positron emission tomography drugs) for administration to...