PART 314—APPLICATIONS FOR FDA APPROVAL TO MARKET A NEW DRUG
- SUBPART A—General Provisions (§314.1 to §314.3)
- SUBPART B—Applications (§314.50 to §314.91)
- SUBPART C—Abbreviated Applications (§314.92 to §314.99)
- SUBPART D—FDA Action on Applications and Abbreviated Applications (§314.100 to §314.170)
- SUBPART E—Hearing Procedures for New Drugs (§314.200 to §314.235)
- SUBPART G—Miscellaneous Provisions (§314.410 to §314.445)
- SUBPART H—Accelerated Approval of New Drugs for Serious or Life-Threatening Illnesses (§314.500 to §314.560)
- SUBPART I—Approval of New Drugs When Human Efficacy Studies Are Not Ethical or Feasible (§314.600 to §314.650)