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

Our long-term alliance with a top tier global CRO provides us in-depth understanding of local requirements while keeping the flexibility needed to compete with the largest CROs.

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 

ICPE2022

OXON AT ICPE Conference – 24-28 August2022

OXON’s real-world studies at the 38th International Conference on PharmacoEpidemiology, ICPE 2022.  Advancing Pharmacoepidemiology and Real-World Evidence for the Global Community August 24-28, 2022 | Bella Center Copenhagen | Copenhagen, Denmark[…]

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OXON Masterclasses

OXON’s FREE LIVE ONLINE REAL WORLD MASTERCLASS SERIES 2022-2023

FREE LIVE REAL WORLD MASTERCLASS SERIES 2022-2023 ‘How to ensure success and avoid pitfalls in Real World studies by Understanding Healthcare in Europe and Asia’ Dates: Monthly starting in February[…]

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ICPE2021

OXON at ICPE21 All Access Virtual Conference on 23-25 August, 2021

OXON is delighted to be supporting ICPE again this year with a virtual exhibition booth from which we will be happy to speak with you about our specialisation in data collection, secondary data and hybrid real world studies, pragmatic trials and meta-analyses to help plan, design and implement RWE for safety, market access and drug development.

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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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