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Access & Impact

Turning Access into Impact

The scale of challenge in accessing medicines for
rare diseases across Europe is significant.

Fewer than
0
%

EFPIA Patients W.A.I.T. Indicator 2024 Survey Published May 2025

of all EMA approved orphan medicines are available in all 27 EU member states

By applying intelligent new approaches to market access, we identify opportunities to broaden patient access to medicines.

Our Approach

How We Create Access

01
60 days

Identify Access Gaps

Health analytics led with modelling completed within 60 days

02
120 days

Act Quickly

Defined action plan with commercial partner agreements often within 120 days

03
120 days

Partner to Deliver Impact

Robust supply chain integrated into local healthcare system and launch readiness within 120 days

Beyond Medicines

Value for Health Systems & Payors

Our approach delivers value beyond medicines for patients, healthcare professionals and healthcare systems.

  • Supporting patients to get the most from their medicines
  • Supporting clinician-patient conversations
  • Championing sustainable access to rare disease medicines