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PHARMO Institute

Your Global Partner for Coordinating Multi-Country Real-World Database Studies

Advancing Health Through Evidence

PHARMO Institute, part of Lumanity, delivers high-quality, real-world research to help the healthcare industry understand how medicines perform beyond the clinical trial setting. Since 1999, we have been analyzing healthcare data to identify side effects earlier, improve patient safety and outcomes, and guide better treatment decisions.

With direct access to unique Dutch healthcare databases and strong global partnerships, PHARMO offers a combination of local expertise and international reach that produces fast, reliable, and actionable evidence.
Expertise You Can Rely On

Our team of specialists in epidemiology, statistics, and data science, deliver tailor-made observational studies that answer complex research questions about safety, effectiveness, and the value of medicines.

We provide:

  • Post-authorization safety and efficacy studies (PASS, PAES)
  • Drug utilization studies (DUS)
  • Incidence, prevalence, treatment patterns, and patient pathways
  • Comparative effectiveness studies, including synthetic control arms
  • Healthcare resource use and cost of illness research
  • AI-driven patient finding, classification, and disease progression analysis

All projects follow internationally recognized standards, including the ENCePP Guide on Methodological Standards, the ENCePP Code of Conduct, and Good Pharmacovigilance Practice guidelines. PHARMO is an certified research organization.

Rich, Linked Data for Powerful Insights

PHARMO has direct access to anonymized patient-level data from multiple healthcare settings in the Netherlands, linked through validated algorithms.

Our data sources include:

  • General practitioners
  • Hospitals (admissions, ambulatory visits, high-cost medicines)
  • Clinical laboratories
  • Community and hospital pharmacies
  • Specialized registries (pathology, cancer, perinatal care)

At a glance

This integrated dataset supports research into slow-progressing illnesses, rare diseases, and conditions requiring multi-setting care—areas often unaddressable by other secondary databases.
250
Million person-years of data
14
Million patients
1,400
Practices, hospitals, pharmacies, and labs
Global Reach, Local Insight

PHARMO collaborates with leading and researchers worldwide to deliver multi-country studies that meet the highest standards of quality and transparency.

We are a founding member of the SIGMA Consortium, an alliance of European ENCePP research centers providing:

  • Single-point coordination for multi-country pharmacoepidemiologic and real-world evidence studies
  • Common study protocols and programming
  • Quality-assured delivery
  • Access to 10 of the top 15 secondary databases used in European PASS studies

Additionally, PHARMO is part of ENCePP, SIGMA, VAC4EU, and EU PPV.

Why Work With PHARMO?

Medicines can affect people differently depending on biology, lifestyle, and healthcare context. We help uncover the reasons and patterns behind these differences, providing the clarity needed for better health decisions.

Scientific rigor
Academically trained researchers applying the right methodologies for each challenge
Global collaboration
Coordinated multi-country studies with consistent quality
Proven track record
Decades of delivering trusted evidence for regulators, payers, and healthcare providers
Explore our publications

Browse PHARMO’s publications to see the impact of our work across therapeutic areas.