Reporting of Adverse Experiences

  1. Law
  2. CFR 21
  3. Food and Drugs
  4. Food and Drug Administration, Department of Health and Human Services
  5. Biologics
  6. Biological Products: General
  7. Reporting of Adverse Experiences

Checkout our iOS App for a better way to browser and research.

Section
600.80

Postmarketing reporting of adverse experiences.

Section
600.81

Distribution reports.

Section
600.82

Notification of a permanent discontinuance or an interruption in manufacturing.

Section
600.90

Waivers.