1. Collections
  2. Code of Federal Regulations
  3. Title 21
  4. Chapter I
  5. Subchapter D
  6. Part 310

Subpart D

Records and Reports

310.305Records and reports concerning adverse drug experiences on marketed prescription drugs for human use without approved new drug applications.310.306Notification 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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