Key Topics Include:
- Meeting Safety Requirement: Regulator’s Perspective
- Building a Pharmacovigilance Strategy
- Evolving PV Strategies for Tomorrow
- Technological Advancement in Pharmacovigilance
- Clinical Data Management
- The Role of Big Data and Social Media in PV
- Ensure Drug Safety & Risk Minimisation Measures
- Latest Development & Innovation Approach for Effective Signal Management
- Development of Qualified Personal Responsible for Pharmacovigilance (QPPV)
- Pharmacovigilance for Advanced Therapies
Who Will Attend?
Attendees will be drawn primarily from pharmaceutical, biotechnology and contract research organisations and include VPs, Directors and Managers/Scientists working in Drug Safety, Pharmacovigilance, Epidemiology, Clinical Research and Development, Clinical Trial Management, Pharmacology, Regulatory Affairs and Compliance, Strategy and Business Development, Risk Management, QPPV.