Phase IV Clinical Trial

Clinical

Post-marketing surveillance studies conducted after drug approval. Detect rare adverse events, evaluate long-term safety, explore new indications, and study drug use in special populations.

  • REMS requirements
  • Observational studies
  • Registry-based studies

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Post-marketing surveillance studies conducted after drug approval. Detect rare adverse events, evaluate long-term safety, explore new indications, and study drug use in special populations.