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Table of Contents

Chapter I: FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES

Subchapter A: General


Part 2: General administrative rulings and decisions


Subpart A: General provisions


21 CFR 2.10 - Examination and investigation samples.

21 CFR 2.19 - Methods of analysis.

21 CFR 2.5 - Imminent hazard to the public health.

Subpart B: Human and animal foods


21 CFR 2.25 - Grain seed treated with poisonous substances; color identification to prevent adulteration of human and animal food.

21 CFR 2.35 - Use of secondhand containers for the shipment or storage of food and animal feed.

Subpart F: Caustic poisons


21 CFR 2.110 - Definition of ammonia under Federal Caustic Poison Act.

Subpart G: Provisions applicable to specific products subject to the federal food, drug, and cosmetic act


21 CFR 2.125 - Use of ozone-depleting substances in foods, drugs, devices, or cosmetics.

Part 20: Public information


Subpart A: Official testimony and information


21 CFR 20.1 - Testimony by Food and Drug Administration employees.

21 CFR 20.2 - Production of records by Food and Drug Administration employees.

21 CFR 20.3 - Certification and authentication of Food and Drug Administration records.

Subpart B: General policy


21 CFR 20.20 - Policy on disclosure of Food and Drug Administration records.

21 CFR 20.21 - Uniform access to records.

21 CFR 20.22 - Partial disclosure of records.

21 CFR 20.23 - Request for existing records.

21 CFR 20.24 - Preparation of new records.

21 CFR 20.25 - Retroactive application of regulations.

21 CFR 20.26 - Indexes of certain records.

21 CFR 20.27 - Submission of records marked as confidential.

21 CFR 20.28 - Food and Drug Administration determinations of confidentiality.

21 CFR 20.29 - Prohibition on withdrawal of records from Food and Drug Administration files.

21 CFR 20.30 - Food and Drug Administration Freedom of Information Staff.

21 CFR 20.31 - Retention schedule of requests for Food and Drug Administration records.

21 CFR 20.32 - Disclosure of Food and Drug Administration employee names.

21 CFR 20.33 - Form or format of response.

21 CFR 20.34 - Search for records.

Subpart E: Limitations on exemptions


21 CFR 20.80 - Applicability of limitations on exemptions.

21 CFR 20.81 - Data and information previously disclosed to the public.

21 CFR 20.82 - Discretionary disclosure by the Commissioner.

21 CFR 20.83 - Disclosure required by court order.

21 CFR 20.84 - Disclosure to consultants, advisory committees, State and local government officials commissioned pursuant to 21 U.S.C. 372(a), and other special government employees.