CRO Services
As your Contract Research Organization, OXON helps plan and implement the generation of Real-World evidence for safety, market access/HEOR and drug development.
KNOW MORELate-phase studies
We help pharmaceutical, biotech and medical device companies to cost-effectively meet the requirements of late-phase clinical studies for better outcomes or greater value.
KNOW MORETherapeutic Areas
OXON offers proven experience and a large portfolio of studies in all major therapy areas, including orphan conditions, pregnancy, and risk minimization.
KNOW MOREReal World Evidence and Late-Phase Research
OXON has been selected as a preferred provider by several big pharma companies.
With strong links to EMA and world-renowned academics and institutions in Europe and Asia for studies and teaching, OXON offers proven experience and a large portfolio of studies in all major therapeutic areas.
OXON conducts:
• Primary data studies: prospective, registries, retrospective chart review, cross-sectional, surveys and pragmatic trials
• Secondary data studies: electronic records and registries
• Hybrid studies, including external controls for orphan medicines
• Synthesis research: systematic review and aggregate and IPD meta-analysis and landscaping
• Data analysis, modelling and simulation
OXON Exhibiting at ISPOR Europe 2026
Generating RWE for Better Healthcare Decisions: OXON at ISPOR Europe 2026 8–11 November 2026 | Austria Center Vienna, Austria | Booth #831 How can real-world data provide the evidence needed[…]
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Advancing Rare Disease Research at WODC Europe 2026
Advancing evidence generation for rare diseases and orphan drug development 27–29 October 2026 | RAI Amsterdam, The Netherlands OXON Epidemiology will be attending World Orphan Drug Congress Europe 2026, a[…]
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OXON AT ESMO CONGRESS 2026
OXON Epidemiology at ESMO Congress 2026: From Real-World Data to Reliable Evidence 23–27 October 2026 | IFEMA Madrid, Spain | Booth #8085, Hall 8 OXON Epidemiology will be exhibiting at[…]
Read moreWe strive our best to support our clients in conducting cost-efficient observational studies worldwide
We pulled together
professionals and resources
to serve you better
READ MORELet us help design and conduct your optimal PASS or Outcomes observational study
OXON IS YOUR RWE OBSERVATIONAL STUDIES SERVICE PROVIDER
OXON epidemiologists, statisticians, clinicians and project managers (ex-big pharma, ex-EMA), supported by consultancy from Stuart Pocock, Professor of Medical Statistics, London School of Hygiene & Tropical Medicine (´Pocock Stopping Rule´, sat on many data monitoring committees, extensive experience with EMA and FDA, classic textbook ´Clinical Trials´, >600 papers (100+ NEJM/Lancets)
REQUEST A MEETINGWe are a partner centre of the ENCePP scientific network, which is coordinated by the European Medicines Agency. We are dedicated to excellence in research by adhering to the ENCePP Guide on Methodological Standards and promoting scientific independence and transparency. We register studies in the EU PAS Register, a publicly accessible resource for the registration of pharmacoepidemiological and pharmacovigilance studies