Join this live webinar to learn more.
As FDA guidance raises expectations for broader access and more representative enrollment, biotech sponsors are being challenged to rethink traditional site feasibility. Historical enrollment metrics within large research centers/providers are no longer enough. Today’s trials must reach patients where they live and that means redefining what “site readiness” truly looks like.
This webinar will explore how community-based research models are reshaping trial planning and execution, including:
- How to evaluate real-world patient access beyond legacy enrollment data
- Infrastructure and scalability considerations in community settings
- How patient concierge services can reduce barriers and improve participation
Join Syneos Health experts for a practical discussion on building trial strategies that align with regulatory expectations and real-world patient needs.
Offered Free by: Syneos Health
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