Overview:
This workshop explores pharmacovigilance, the science of monitoring drug safety and adverse effects to protect patients and the public. Participants will gain insights into ADR detection, signal management, safety reporting systems, and the latest innovations including AI and big data in pharmacovigilance.

Learning Objectives:

• Define pharmacovigilance and its role in patient safety

• Detect, assess, and prevent adverse drug reactions (ADRs)

• Apply international ADR reporting systems (WHO, FDA, EMA)

• Analyze case studies in pharmacovigilance practice

• Understand legal, ethical, and regulatory frameworks

• Explore innovations in AI and post-marketing surveillance

Who Should Attend:

• Healthcare professionals (physicians, pharmacists, nurses), clinical researchers, regulators, pharmacovigilance officers, and pharmaceutical industry professionals.

Duration & Format:

• 1-day workshop with case studies and group activities.

• CME/CPD credits: 6 credits