Site Feedback

Title 21

Displaying title 21, up to date as of 4/17/2024. Title 21 was last amended 4/15/2024.
eCFR Content

The Code of Federal Regulations (CFR) is the official legal print publication containing the codification of the general and permanent rules published in the Federal Register by the departments and agencies of the Federal Government. The Electronic Code of Federal Regulations (eCFR) is a continuously updated online version of the CFR. It is not an official legal edition of the CFR.

Learn more about the eCFR, its status, and the editorial process.

Title 21Food and DrugsPart / Section
Chapter IFood and Drug Administration, Department of Health and Human Services1 – 1299
Subchapter AGeneral1 – 99
Part 26Mutual Recognition of Pharmaceutical Good Manufacturing Practice Reports, Medical Device Quality System Audit Reports, and Certain Medical Device Product Evaluation Reports: United States and the European Community26.0 – 26.81
§ 26.0General.
Subpart ASpecific Sector Provisions for Pharmaceutical Good Manufacturing Practices26.1 – 26.21
Subpart BSpecific Sector Provisions for Medical Devices26.31 – 26.50
Subpart C“Framework” Provisions26.60 – 26.81