Code of Federal Regulations (Last Updated: November 8, 2024) |
Title 21 - Food and Drugs |
Chapter I - Food and Drug Administration, Department of Health and Human Services |
SubChapter A - General |
Part 20 - Public Information |
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. |