Code of Federal Regulations · Subpart

Subpart D — Records And Reports

21 C.F.R. pt. 310, subpt. D

• § 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