Rare disease trials face unique challenges — limited patient populations, fragmented care pathways, and highly specialized treatment centers make traditional site selection approaches ineffective.
In this on-demand webinar, rare disease experts explore how integrating patient insights into feasibility and site selection can improve enrollment accuracy, reduce activation risk, and strengthen operational execution. You’ll learn how understanding real-world patient journeys, advocacy networks, and care pathways helps identify sites with genuine patient access — not just prior trial experience.
Key takeaways include:
- Why rare disease site selection requires a different methodology
- How patient insights improve feasibility and enrollment forecasting
- The role of advocacy and community engagement
- Practical strategies to strengthen trial execution
In rare disease research, every patient matters. A patient-informed site strategy ensures recruitment plans reflect reality — not assumptions. Watch the webinar recording to optimize your rare disease site selection approach.