Pharmacovigilance World 2026

Pharmacovigilance-World-2026

We are delighted to welcome you to the Pharmacovigilance World 2026, and we are confident that your active participation will contribute to the advancement of drug safety practices. Together, let us strive towards a safer and more vigilant healthcare system that prioritizes patient well-being and ensures the continued benefit of medications worldwide.

As medical science advances, so does our understanding of drug safety and the need for vigilance when it comes to monitoring its usage. In recent years, pharmacovigilance has gained significant attention and importance due to the growing complexity of drug therapies, the emergence of new medicines, and the increased scrutiny of regulatory agencies. This has led to a greater emphasis on monitoring the safety profiles of pharmaceutical products throughout their lifecycle, from pre-marketing clinical trials to post-marketing surveillance.

Scientific Sessions

Signal Detection & Management
Regulatory Intelligence & Global Harmonization
Automation in Case Processing
Risk Management Plans (RMPs)
Benefit-Risk Evaluation
Post-Marketing Surveillance
PV Systems & Quality Management
PV Outsourcing & Vendor Oversight
Patient-Centric Drug Safety
Medical Device Safety & Combination Products
PV in Clinical Trials
Labeling and Safety Communication
AI/ML in Pharmacovigilance
Global Safety Databases & Data Standardization
PV Audits, Inspections & Readiness

Important Dates
Abstract Submission Opens12/12/2025
Abstract Submission Deadline30/04/2026
Abstract Submission Closes30/04/2026
Registration Opens12/12/2025
Registration Deadline15/06/2026
Registration Closes15/06/2026
on spot registration16/06/2026
Date formats: d/m/y
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