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.
