Pharmacovigilance · Pharmacology

Which document must manufacturers regularly submit to regulatory authorities summarizing accumulated post-marketing safety data on an approved drug?

  1. Case report form
  2. Periodic safety update report
  3. Investigational new drug application
  4. Package insert draft
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Correct answer: Periodic safety update report

A Periodic Safety Update Report (PSUR) provides updated safety data on marketed drugs. It includes information on new adverse events and risk-benefit evaluations over time.

Difficulty: Medium Question 11 of 20

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