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Office of Surveillance and Epidemiology (OSE) - Programs and Activities

Office of Surveillance and Epidemiology (OSE) Home

  • Patient Labeling and Risk Communication
  • Medication Guides
  • Drug Safety and Risk Management (DSaRM) Advisory Committee gained full committee status on June 1, 2002.
  • MedWatch  MedWatch, the FDA Safety Information and Adverse Event Reporting Program, provides safety information for all FDA-regulated medical products (drugs, biologics, medical devices, and dietary supplements) to both healthcare professionals and the general public. 
    • MedWatch Partners work with FDA to help keep their members informed about medical product safety information