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- 21 CFR 17.31 · Form, filing, and service of papers.
- 21 CFR 17.32 · Motions.
- 21 CFR 17.33 · The hearing and burden of proof.
- 21 CFR 17.34 · Determining the amount of penalties and assessments.
- 21 CFR 17.35 · Sanctions.
- 21 CFR 17.37 · Witnesses.
- 21 CFR 17.39 · Evidence.
- 21 CFR 17.41 · The administrative record.
- 21 CFR 17.43 · Posthearing briefs.
- 21 CFR 17.45 · Initial decision.
- 21 CFR 17.47 · Appeals.
- 21 CFR 17.48 · Harmless error.
- 21 CFR 17.51 · Judicial review.
- 21 CFR 17.54 · Deposit in the Treasury of the United States.
- 21 CFR 19.1 · Scope.
- 21 CFR 19.5 · Reference to Department regulations.
- 21 CFR 19.6 · Code of ethics for government service.
- 21 CFR 19.10 · Food and Drug Administration Conflict of Interest Review Board.
- 21 CFR 19.21 · Duty to report violations.
- 21 CFR 19.45 · Temporary disqualification of former employees.
- 21 CFR 19.55 · Permanent disqualification of former employees.
- 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.
- 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 · Electronic availability and 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 Division of Freedom of Information.
- 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.
- 21 CFR 20.40 · Filing a request for records.
- 21 CFR 20.41 · Time limitations.
- 21 CFR 20.42 · Aggregation of certain requests.
- 21 CFR 20.43 · Multitrack processing.
- 21 CFR 20.44 · Expedited processing.
- 21 CFR 20.45 · Fees to be charged.
- 21 CFR 20.46 · Waiver or reduction of fees.
- 21 CFR 20.47 · Situations in which confidentiality is uncertain.
- 21 CFR 20.48 · Judicial review of proposed disclosure.
- 21 CFR 20.49 · Denial of a request for records.
- 21 CFR 20.50 · Nonspecific and overly burdensome requests.
- 21 CFR 20.51 · Referral to primary source of records.
- 21 CFR 20.52 · Availability of records at National Technical Information Service.
- 21 CFR 20.53 · Use of private contractor for copying.
- 21 CFR 20.54 · Request for review without copying.
- 21 CFR 20.55 · Indexing trade secrets and confidential commercial or financial information.
- 21 CFR 20.60 · Applicability of exemptions.
- 21 CFR 20.61 · Trade secrets and commercial or financial information which is privileged or confidential.
- 21 CFR 20.62 · Inter- or intra-agency memoranda or letters.
- 21 CFR 20.63 · Personnel, medical, and similar files, disclosure of which constitutes a clearly unwarranted invasion of personal privacy.
- 21 CFR 20.64 · Records or information compiled for law enforcement purposes.
- 21 CFR 20.65 · National defense and foreign policy.
- 21 CFR 20.66 · Internal personnel rules and practices.
- 21 CFR 20.67 · Records exempted by other statutes.
- 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.
- 21 CFR 20.85 · Disclosure to other Federal Government departments and agencies.
- 21 CFR 20.86 · Disclosure in administrative or court proceedings.
- 21 CFR 20.87 · Disclosure to Congress.
- 21 CFR 20.88 · Communications with State and local government officials.
- 21 CFR 20.89 · Communications with foreign government officials.
- 21 CFR 20.90 · Disclosure to contractors.
- 21 CFR 20.91 · Use of data or information for administrative or court enforcement action.
- 21 CFR 20.100 · Applicability; cross-reference to other regulations.
- 21 CFR 20.101 · Administrative enforcement records.
- 21 CFR 20.102 · Court enforcement records.
- 21 CFR 20.103 · Correspondence.
- 21 CFR 20.104 · Summaries of oral discussions.
- 21 CFR 20.105 · Testing and research conducted by or with funds provided by the Food and Drug Administration.
- 21 CFR 20.106 · Studies and reports prepared by or with funds provided by the Food and Drug Administration.
- 21 CFR 20.107 · Food and Drug Administration manuals.
- 21 CFR 20.108 · Agreements between the Food and Drug Administration and other departments, agencies, and organizations.
- 21 CFR 20.109 · Data and information obtained by contract.
- 21 CFR 20.110 · Data and information about Food and Drug Administration employees.
- 21 CFR 20.111 · Data and information submitted voluntarily to the Food and Drug Administration.
- 21 CFR 20.112 · Voluntary drug experience reports submitted by physicians and hospitals.
- 21 CFR 20.113 · Voluntary product defect reports.
- 21 CFR 20.114 · Data and information submitted pursuant to cooperative quality assurance agreements.
- 21 CFR 20.115 · Product codes for manufacturing or sales dates.
- 21 CFR 20.116 · Drug and device registration and listing information.
- 21 CFR 20.117 · New drug information.
- 21 CFR 20.118 · Advisory committee records.
- 21 CFR 20.119 · Lists of names and addresses.
- 21 CFR 20.120 · Records available in Food and Drug Administration Public Reading Rooms.
- 21 CFR 21.1 · Scope.
- 21 CFR 21.3 · Definitions.
- 21 CFR 21.10 · Policy concerning records about individuals.
- 21 CFR 21.20 · Procedures for notice of Food and Drug Administration Privacy Act Record Systems.