ABOUT THE WORKSHOP
Registries are increasingly used across the health care system for: data reimbursement,
pharmacovigilance, epidemiology, and effectiveness, to name a few. While EMA is calling for early design of registries for conditional approval, challenges remain in terms of ambiguity of structured data collection from existing sources, and for balancing data privacy and ownership.
This meeting addresses fundamental questions about registries, existing guidelines and gaps, how to keep abreast of challenges, and how to utilise registries for the most effective outcomes.
WHY EXHIBIT?
This is your opportunity to highlight how your products and services can address the current challenges of registries and how to prepare organisations for future improvements.
- Capture your audience while they are actively investigating solutions
- Foster in-person connections with Pharmacovigilance experts
- Highlight your capabilities to address differences between US and EU registries
- Collect new leads for new business opportunities - Deliver progress. Be a part of the system evolution
WHO WILL YOU MEET?
You will meet people employed in such roles as:
- Associate Director Pharmacovigilance and Risk Management
- Deputy QPPV
- Risk Management & Business Process Management Practice
- Medical Safety Officer
- Pharmacovigilance Assessor
- Pharmacovigilance Officer
- Pharmacovigilance Technician
- QPPV
- Senior Clinical Safety Manager
- Senior Global Medical Science Lead
- Compliance Specialist
- Epidemiologists
- Medical affairs
EXHIBITING AND HOSTING OPPORTUNITIES
Please download our prospectus for an exhibitor application form and for further information on available exhibiting and hosting opportunities.
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