Risk Management

Activity that aims to ensure that the benefits of a medicinal product exceed the risks by the greatest achievable margin, by increasing the benefits or reducing the risks in three stages:

  • Characterization of the safety profile of the medicinal product
  • Planning of pharmacovigilance activities to identify and characterize risks
  • Risk minimization and mitigation, assessment of the effectiveness of these activities


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The Life Sciences glossary with terminology, acronyms, for regulatory, quality, compliance, clinical trials, and pharmacovigilance software.

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