Risk Management

Pharma Risk Management was designed as a set of Pharmacovigilance activities and interventions designed to identify, characterise, prevent or minimise risks of medicinal and therapeutic products including the assessment of the effectiveness of their clinical reactions, interventions and combination therapies. Drug industry need to promote companies in Pharmacovigilance practice to use information technology and provide efficient software to implement the risk minimisation plans in drug development and manufacture. Pharmaceutical risk management monitors unlicensed, off labels and orphan drugs ,risk management labelling, regulatory decisions, legal protection, intellectual property, enforcement, marketing, and company reputation.

  • Information Technology in Pharmacoepidemiology and Clinical Trials
  • Review of Softwares used in Pharmacovigilance and Clinical Trials
  • Risk Communication: Interface between Pharmaepidemiology, Sales and Marketing
  • Monitoring Unlicensed, off labels and Orphan Drugs
  • Implementation of Risk Minimization Plans
  • Therapeutic Drug Management
  • Risk Evaluation and Mitigation Strategies

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