Subpart D—Records and Reports

1. CFR
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3. Title 21
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5. Chapter I
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7. Part 310
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9. Subpart D

Sections

• 310.305
  § 310.305 Records and reports concerning adverse drug experiences on marketed prescription drugs for human use without approved new drug applications.
• 310.306
  § 310.306 Notification of a permanent discontinuance or an interruption in manufacturing of marketed prescription drugs for human use without approved new drug applications.