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.

Speakers

Dr Chantal W.M. van Gils

VP Evidence & Value

Mel Walker

CEO & Founder, Access InVivo

LET’S TALK

You don't have to go it alone!

Our experienced team has been there before, and we're ready to guide you through the unknown. Share your challenges with us, and together, we'll create a plan to efficiently reach your milestones and turn your vision into reality.

Building better Biotechs