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The European orphan drug market is growing rapidly, offering U.S. biotech companies a significant opportunity for expansion. However, navigating the region’s complex regulatory, pricing, and reimbursement landscapes requires a strategic approach.

In this exclusive guide, we cover:

  • Key regulatory pathways and market entry considerations for orphan drugs in Europe
  • How to leverage early access programs and real-world data for market adoption
  • The benefits of partnering with European specialists to streamline distribution and compliance
  • Best practices for patient engagement, advocacy, and long-term market success

Download this guide to learn how to successfully commercialize your orphan drug in Europe, ensuring both patient impact and commercial viability.

Sciensus

About Sciensus

Sciensus is a proven life sciences solutions partner with more than 30 years’ experience in navigating and unlocking the complex European healthcare ecosystem to maximise patient reach. We help accelerate the development journey, bringing medicines into the market and directly to patients to improve health outcomes. Through cutting-edge patient engagement programmes, offering an exclusive combination of skilled in-person care and digital support, we help patients make the most of their treatment and generate real-world evidence that can be used to improve treatment pathways.

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