The DIA Registry Workshop - Preparing for Future Requirements 2017 covers topics such as:
- Equip yourself and your teams with the right knowledge and the right tools
- Best practices with key opinion leaders
- Define a clear plan for data collection prior to marketing approval
- Fine-tune an optimal solution for patient & disease registries
- Enhance the functionality and usefulness of data from registries
- Future increases in observational data
The DIA Registry Workshop - Preparing for Future Requirements 2017 brings together:
- QPPVs / Deputy QPPVs
- Associate Directors of Pharmacovigilance and Risk Management
- Pharmacovigilance Officers
- Pharmacovigilance Assessors
- Medical Safety Officers
- Pharmacovigilance Technicians
- Senior / Global / Medical Science Leads
- Senior / Clinical Safety Managers
- Epidemiologists
- Compliance Specialists
- Risk Management & Business Process Management Professionals
- Medical Affair Experts