21 CFR Subpart F
Availability of Specific Categories of Records
June 25, 2020
§
20.100
Applicability; cross-reference to other regulations
§
20.106
Studies and reports prepared by or with funds provided by the Food and Drug Administration
§
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
§
20.107
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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