Pharmacovigilance USA 2025

The Pharmacovigilance USA 2025 is dedicated to pharmacovigilance, regulatory affairs, risk management & clinical trials.

Topics

• Auditing a Global Safety Database
• The Future of Pharmacovigilance in a Digital World
• Integrating Innovation in Pharmacovigilance Practices
• Big Data/Use of AI in Pharmacovigilance
• AI-Powered Pharmacovigilance System
• Patient-Centered Approaches in Pharmacovigilance
• Predictive Analytics in Risk Management
• Global Collaboration in Pharmacovigilance
• Pharmacovigilance in Personalized Medicine
• Real-World Data Integration in Clinical Trials
• The Role of Real-World Evidence in Regulatory Decision Making
• Enhancing Pharmacovigilance with Mobile Health Technologies
• Challenges in Pharmacovigilance Data Collection
• Future Trends in Regulatory Affairs
• Pharmacovigilance Best Practices in Post-Marketing Surveillance
• Utilizing Blockchain for Drug Safety
• Drug Safety Alerts

Who should Attend

Senior attendees from biopharmaceutical, pharmaceutical, diagnostics, biotechnology, CRO and solution provider companies.