Code of Federal Regulations · Part

Part 99 — Dissemination Of Information On Unapproved/new Uses For Marketed Drugs, Biologics, And Devices

21 C.F.R. pt. 99

• Subpart A General Information
• Subpart B Information To Be Disseminated
• Subpart C Manufacturer's Submissions, Requests, And Applications
• Subpart D Fda Action On Submissions, Requests, And Applications
• Subpart E Corrective Actions And Cessation Of Dissemination
• Subpart F Recordkeeping And Reports