Real World Data
Clinical knowledge at your fingertips.

Understand patients and the performance of treatments in the real world
The Wemedoo real-world data framework encompasses a complete ecosystem of expert services and software solutions dedicated to the collection, management, and analysis of real-world data.
The Wemedoo real-world data framework encompasses a complete ecosystem of expert services and software solutions dedicated to the collection, management, and analysis of real-world data.
Benefits.
Cost Reduction.
Reduce research and product development cost.
Acceleration.
Accelerate development of treatments and interventions.
Safety Increase.
Improve safety assessments.
Coverage.
Expand coverage of rare diseases and conditions.
Power your traditional, decentralized, or synthetic trials with unique real-world data collected by a global network of experienced clinical data professionals from a global, broad, and diverse patient population.


27
CROs
96
Countries
>25
Therapeutic Areas
8,856
Sites
We provide custom validated real-world data from a uniquely broad and diverse population across countries on 5 continents to meet all client needs and requirements.
Treatment data are always connected to patient outcomes and direct access to patients is provided, both to ensure industry leading results.
With custom genetic analysis, general OMICS, and interpretation of medical imaging directly from all sites, unmatched real-world insights and evidence are ensured.
Base your studies on the best possible data and generate meaningful evidence and insights.

Patient diversity and inclusion ensured, especially for rare diseases with small patient populations

Genomic profiling and advanced diagnostics available directly on most sites

Patient reported outcomes available for prospective studies

OMOP and CDISC compliance ensured

Semantic, syntactic and medical interoperability ensured

All data sets are fully machine readable

Patient consent is ensured for every data set if required

Regulatory compliance ensured in every country

Data collected with same standards as in clinical trials