This session moves beyond explaining the EU HTA Regulation to focus on how it is actually playing out, and what small and mid-size biotechs should do now. It draws on early signals and open questions to support actionable, defensible evidence and prioritization decisions. The discussion connects EU HTA readiness directly to market access risk, evidence strategy, and partnering value.
In this session, our experts will cover:
- Why EU HTA matters beyond compliance and how it affects access and deal value
- Early observations from JSC/JCA activity: what’s clearer, what’s not
- When JSC makes sense—and credible alternatives when it doesn’t
- Evidence prioritization for resource-constrained teams
- The impact of evidence choices on partnering and deal value
Key takeaway: EU HTA is shifting value decisions earlier than many biotechs expect. Focusing on the right evidence can strengthen access, partnerships, and long-term value.