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Regulations last checked for updates: Nov 22, 2024
Title 21 - Food and Drugs last revised: Nov 19, 2024
All Titles
Title 21
Chapter I
Part 20
Subpart F - Subpart F—Availability of Specific Categories of Records
§ 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.
authority:
5 U.S.C. 552
;
18 U.S.C. 1905
;
19 U.S.C. 2531-2582
;
21 U.S.C. 321-393
,
1401
;
42 U.S.C. 241
,
242
,
242
a,
242
l,
242
n,
243
,
262
,
263
,
263
b-263n,
264
,
265
,
300u
,
300aa
source:
42 FR 15616, Mar. 22, 1977, unless otherwise noted.
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