Code of Federal Regulations · Part

Part 314 — Applications For Fda Approval To Market A New Drug

21 C.F.R. pt. 314

• Subpart A General Provisions
• Subpart B Applications
• Subpart C Abbreviated Applications
• Subpart D Fda Action On Applications And Abbreviated Applications
• Subpart E Hearing Procedures For New Drugs
• Subpart F Subpart F [reserved]
• Subpart G Miscellaneous Provisions
• Subpart H Accelerated Approval Of New Drugs For Serious Or Life-threatening Illnesses
• Subpart I Approval Of New Drugs When Human Efficacy Studies Are Not Ethical Or Feasible