ICPRA -2025

March 24-26, 2025   Rome, Italy
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Topics

ICPRA -2025 provides leading forum for the presentation of new advances and research results in the fields of Pharmacovigilance and Regulatory Affairs. Accordingly , Topics of interest for submission include, but are not limited to:

  • Pharmacovigilance and Eudravigilance
  • Introduction to Pharmacovigilance (PV)
  • Identification of Risk Factors
  • Good Drug Development Practices
  • Post-marketing surveillance
  • Big data and AI in pharmacovigilance
  • Drug legislation and regulations
  • Benefit-risk management strategies
  • Concept of drug safety
  • Importance of HIV testing for early detection
  • Adverse drug Reactions Reporting
  • Harmonization and pharmaceutics
  • Innovative approaches to drug safety
  • PV Regulations and Challenges
  • Medical Devices Safety
  • Adverse Drug Reactions
  • Big data and AI in Drug Surveillance
  • Patient Centric Drug Safety
  • Drug Testing Workflows with AI & Automation
  • Safety Signals & Management

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