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U.S. Code Regulations Constitution Journal Apps
  1. Regulations
    All Titles
  2. title 21
    Food and Drugs
  3. chapter I-i4
    CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)
  4. part 310
    PART 310—NEW DRUGS
  5. subpart D
    Subpart D—Records and Reports

Subpart D. Subpart D—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.
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