SUBPART F—Availability of Specific Categories of Records (§20.100 to §20.120)
- 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 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.