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Title 21

Displaying title 21, up to date as of 9/03/2026. Title 21 was last amended 8/31/2026.
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  1. Title 21 —Food and Drugs
  2. Chapter I —Food and Drug Administration, Department of Health and Human Services
  3. Subchapter A —General
  4. Part 20 —Public Information
  5. Subpart F   View Full Text
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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.

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Title 21Food and DrugsPart / Section
Chapter IFood and Drug Administration, Department of Health and Human Services1 – 1299
Subchapter AGeneral1 – 99
Part 20Public Information20.1 – 20.120
Subpart FAvailability of Specific Categories of Records20.100 – 20.120
§ 20.100Applicability; cross-reference to other regulations.
§ 20.101Administrative enforcement records.
§ 20.102Court enforcement records.
§ 20.103Correspondence.
§ 20.104Summaries of oral discussions.
§ 20.105Testing and research conducted by or with funds provided by the Food and Drug Administration.
§ 20.106Studies and reports prepared by or with funds provided by the Food and Drug Administration.
§ 20.107Food and Drug Administration manuals.
§ 20.108Agreements between the Food and Drug Administration and other departments, agencies, and organizations.
§ 20.109Data and information obtained by contract.
§ 20.110Data and information about Food and Drug Administration employees.
§ 20.111Data and information submitted voluntarily to the Food and Drug Administration.
§ 20.112Voluntary drug experience reports submitted by physicians and hospitals.
§ 20.113Voluntary product defect reports.
§ 20.114Data and information submitted pursuant to cooperative quality assurance agreements.
§ 20.115Product codes for manufacturing or sales dates.
§ 20.116Drug and device registration and listing information.
§ 20.117New drug information.
§ 20.118Advisory committee records.
§ 20.119Lists of names and addresses.
§ 20.120Records available in Food and Drug Administration Public Reading Rooms.
eCFR Content