Subpart F—Availability of Specific Categories of Records
Sections
-
20.100
§ 20.100 Applicability; cross-reference to other regulations. -
20.101
§ 20.101 Administrative enforcement records. -
20.102
§ 20.102 Court enforcement records. -
20.103
§ 20.103 Correspondence. -
20.104
§ 20.104 Summaries of oral discussions. -
20.105
§ 20.105 Testing and research conducted by or with funds provided by the Food and Drug Administration. -
20.106
§ 20.106 Studies and reports prepared by or with funds provided by the Food and Drug Administration. -
20.107
§ 20.107 Food and Drug Administration manuals. -
20.108
§ 20.108 Agreements between the Food and Drug Administration and other departments, agencies, and organizations. -
20.109
§ 20.109 Data and information obtained by contract. -
20.110
§ 20.110 Data and information about Food and Drug Administration employees. -
20.111
§ 20.111 Data and information submitted voluntarily to the Food and Drug Administration. -
20.112
§ 20.112 Voluntary drug experience reports submitted by physicians and hospitals. -
20.113
§ 20.113 Voluntary product defect reports. -
20.114
§ 20.114 Data and information submitted pursuant to cooperative quality assurance agreements. -
20.115
§ 20.115 Product codes for manufacturing or sales dates. -
20.116
§ 20.116 Drug and device registration and listing information. -
20.117
§ 20.117 New drug information. -
20.118
§ 20.118 Advisory committee records. -
20.119
§ 20.119 Lists of names and addresses. -
20.120
§ 20.120 Records available in Food and Drug Administration Public Reading Rooms.