Site Feedback

Title 21

Displaying title 21, up to date as of 10/14/2026. Title 21 was last amended 10/14/2026.
New Finding Aids are now available on eCFR.gov. The Parallel Table of Authorities, Subject Index, and Agency-prepared Indexes are now online! Learn more
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 FBiologics600 – 680
Part 600Biological Products: General600.2 – 600.90
Subpart AGeneral Provisions600.2 – 600.3
Subpart BEstablishment Standards600.10 – 600.15
Subpart CEstablishment Inspection600.20 – 600.22
Subpart DReporting of Adverse Experiences600.80 – 600.90
Part 601Licensing601.2 – 601.95
Part 606Current Good Manufacturing Practice for Blood and Blood Components606.3 – 606.171
Part 607Establishment Registration and Product Listing for Manufacturers of Human Blood and Blood Products and Licensed Devices607.1 – 607.80
Subpart AGeneral Provisions607.1 – 607.7
Subpart BProcedures for Domestic Blood Product Establishments607.20 – 607.39
Subpart CProcedures for Foreign Blood Product Establishments607.40
Subpart DExemptions607.65
Subpart EEstablishment Registration and Product Listing Of Licensed Devices607.80
Part 610General Biological Products Standards610.1 – 610.68
Part 630Requirements for Blood and Blood Components Intended for Transfusion or for Further Manufacturing Use630.1 – 630.40
Subpart AGeneral Provisions630.1 – 630.3
Subpart BDonor Eligibility Requirements630.5 – 630.35
Subpart CDonor Notification630.40
Part 640Additional Standards for Human Blood and Blood Products640.1 – 640.130
Part 660Additional Standards for Diagnostic Substances for Laboratory Tests660.1 – 660.55
Part 680Additional Standards for Miscellaneous Products680.1 – 680.3
§ 680.1Allergenic Products.
§ 680.2Manufacture of Allergenic Products.
§ 680.3Tests.