Code of Federal Regulations (Last Updated: July 5, 2024) |
Title 21 - Food and Drugs |
Chapter I - Food and Drug Administration, Department of Health and Human Services |
SubChapter D - Drugs for Human Use |
Part 310 - New Drugs |
Subpart D - Records and Reports |
§ 310.303 - Continuation of long-term studies, records, and reports on certain drugs for which new drug applications have been approved. |
§ 310.304 - Drugs that are subjects of approved new drug applications and that require special studies, records, and reports. |
§ 310.305 - Records and reports concerning adverse drug experiences on marketed prescription drugs for human use without approved new drug applications. |
§ 310.306 - Notification of a permanent discontinuance or an interruption in manufacturing of marketed prescription drugs for human use without approved new drug applications. |