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Part 20
FEDERAL · 21 CFR
Part 20 — Public Information
75 sections · Title 21: Food and Drugs
§ 20.1
Testimony by Food and Drug Administration employees.
§ 20.2
Production of records by Food and Drug Administration employees.
§ 20.3
Certification and authentication of Food and Drug Administration records.
§ 20.20
Policy on disclosure of Food and Drug Administration records.
§ 20.21
Uniform access to records.
§ 20.22
Partial disclosure of records.
§ 20.23
Request for existing records.
§ 20.24
Preparation of new records.
§ 20.25
Retroactive application of regulations.
§ 20.26
Electronic availability and indexes of certain records.
§ 20.27
Submission of records marked as confidential.
§ 20.28
Food and Drug Administration determinations of confidentiality.
§ 20.29
Prohibition on withdrawal of records from Food and Drug Administration files.
§ 20.30
Food and Drug Administration Division of Freedom of Information.
§ 20.31
Retention schedule of requests for Food and Drug Administration records.
§ 20.32
Disclosure of Food and Drug Administration employee names.
§ 20.33
Form or format of response.
§ 20.34
Search for records.
§ 20.40
Filing a request for records.
§ 20.41
Time limitations.
§ 20.42
Aggregation of certain requests.
§ 20.43
Multitrack processing.
§ 20.44
Expedited processing.
§ 20.45
Fees to be charged.
§ 20.46
Waiver or reduction of fees.
§ 20.47
Situations in which confidentiality is uncertain.
§ 20.48
Judicial review of proposed disclosure.
§ 20.49
Denial of a request for records.
§ 20.50
Nonspecific and overly burdensome requests.
§ 20.51
Referral to primary source of records.
§ 20.52
Availability of records at National Technical Information Service.
§ 20.53
Use of private contractor for copying.
§ 20.54
Request for review without copying.
§ 20.55
Indexing trade secrets and confidential commercial or financial information.
§ 20.60
Applicability of exemptions.
§ 20.61
Trade secrets and commercial or financial information which is privileged or confidential.
§ 20.62
Inter- or intra-agency memoranda or letters.
§ 20.63
Personnel, medical, and similar files, disclosure of which constitutes a clearly unwarranted invasion of personal privacy.
§ 20.64
Records or information compiled for law enforcement purposes.
§ 20.65
National defense and foreign policy.
§ 20.66
Internal personnel rules and practices.
§ 20.67
Records exempted by other statutes.
§ 20.80
Applicability of limitations on exemptions.
§ 20.81
Data and information previously disclosed to the public.
§ 20.82
Discretionary disclosure by the Commissioner.
§ 20.83
Disclosure required by court order.
§ 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.
§ 20.85
Disclosure to other Federal Government departments and agencies.
§ 20.86
Disclosure in administrative or court proceedings.
§ 20.87
Disclosure to Congress.
§ 20.88
Communications with State and local government officials.
§ 20.89
Communications with foreign government officials.
§ 20.90
Disclosure to contractors.
§ 20.91
Use of data or information for administrative or court enforcement action.
§ 20.100
Applicability; cross-reference to other regulations.
§ 20.101
Administrative enforcement records.
§ 20.102
Court enforcement records.
§ 20.103
Correspondence.
§ 20.104
Summaries of oral discussions.
§ 20.105
Testing and research conducted by or with funds provided by the Food and Drug Administration.
§ 20.106
Studies and reports prepared by or with funds provided by the Food and Drug Administration.
§ 20.107
Food and Drug Administration manuals.
§ 20.108
Agreements between the Food and Drug Administration and other departments, agencies, and organizations.
§ 20.109
Data and information obtained by contract.
§ 20.110
Data and information about Food and Drug Administration employees.
§ 20.111
Data and information submitted voluntarily to the Food and Drug Administration.
§ 20.112
Voluntary drug experience reports submitted by physicians and hospitals.
§ 20.113
Voluntary product defect reports.
§ 20.114
Data and information submitted pursuant to cooperative quality assurance agreements.
§ 20.115
Product codes for manufacturing or sales dates.
§ 20.116
Drug and device registration and listing information.
§ 20.117
New drug information.
§ 20.118
Advisory committee records.
§ 20.119
Lists of names and addresses.
§ 20.120
Records available in Food and Drug Administration Public Reading Rooms.