21 CFR Part 20 - Subpart F - Availability of Specific Categories of Records
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- § 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.