U.S. Code of Federal Regulations

Regulations most recently checked for updates: Aug 28, 2025

All TitlesTitle 21Chapter IPart 20Subpart 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.
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