Subpart F—Availability of Specific Categories of Records

1. CFR
2. ›
3. Title 21
4. ›
5. Chapter I
6. ›
7. Part 20
8. ›
9. Subpart F

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.