CALLE DOCTOR FLEMING, 51 | 28036 MADRID, SPAIN
+34 91 3459395 | +44 (0) 20 3951 8071
info@oxonepi.com

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.

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Late-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.

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Therapeutic Areas

OXON offers proven experience and a large portfolio of studies in all major therapy areas, including orphan conditions, pregnancy, and risk minimization.

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Real 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

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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

World Class Science

Our specialization and high calibre allow us to have clear focus, deep expertise and superior insight to provide concrete results with maximum value to our clients.

Global Reach

We are specialised in multi-country observational studies and provide real-world evidence services worldwide with the expertise and multi-language capabilities of local partners. 

Strong Links

OXON’s services are reinforced with academic links with the London School of Hygiene & Tropical Medicine and with leading academic methodological and clinical consultants.

Long Term Alliances

OXON’s alliances provide global geographical local country operational support, allowing us to compete on a global scale in performing studies projects on both sides of the Atlantic.

We strive our best to support our clients in conducting cost-efficient observational studies worldwide

We pulled together 
professionals and resources to serve you better

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Let us help design and conduct your optimal PASS or Outcomes observational study

OXON IS YOUR 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)

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Newsroom

Read about us, our latest news and events 

Gastro-Cancer

White Paper RWE needs in Oncology: Gastroesophageal Cancer

REAL WORLD EVIDENCE NEEDS IN ONCOLOGY: Gastroesophageal Cancer White Paper based on new trial results from ESMO Congress, 20-24 October 2023, Madrid. The varying nature of gastroesophageal cancer, spanning from[…]

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White-Paper-Colorectal Cancer

White Paper RWE needs in Oncology: Colorectal Cancer

REAL WORLD EVIDENCE NEEDS IN ONCOLOGY: Colorectal Cancer White Paper based on new trial results from ESMO Congress, 20-24 October 2023, Madrid. The complexity of colorectal cancer, spanning from localized,[…]

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White-Paper-Breast-Cancer

White Paper RWE needs in Oncology: Breast Cancer

REAL WORLD EVIDENCE NEEDS IN ONCOLOGY: Breast Cancer White Paper based on new trial results from ESMO Congress, 20-24 October 2023, Madrid. Metastatic breast cancer continues to be a significant[…]

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We 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

ENCePP

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