🇨🇭Swiss Data Privacy & Precision

Real-World Data & Evidence Studies

From Fragmented Datasets to Regulatory-Grade Evidence

Real-world evidence is reshaping regulatory and payer decision-making. oomnia integrates directly with EHR systems, registries, and claims databases through HL7 FHIR and CDISC standards — transforming fragmented real-world data into structured, analysis-ready datasets that meet FDA and EMA submission requirements.

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Real-World Data with oomnia

Real-world data trials are gaining momentum as healthcare stakeholders seek insights that reflect everyday clinical settings. oomnia empowers the design and execution of real-world studies by providing a unified environment for data capture, integration, and continuous monitoring. Whether working with registries, observational studies, or data from routine care, oomnia ensures your real-world evidence is high-quality, traceable, and immediately actionable.

We would love to learn more about your challenges and goals.

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Introducing Our Real-World Data Framework

Wemedoo is member of the Across Global Alliance.We collect unique and tailored real-world data with a global network of clinical data professionals.

Proud to be a part of

Global Alliance of Clinical Research Organizations

Get validated real-world data from a uniquely broad and diverse population across the globe.

Treatment data is directly linked to patient outcomes, with access to patient-reported data where needed.

From genetics and OMICS to imaging, oomnia captures it all, directly from every site, ready for real-world evidence.

16+

CROs

25+

Therapeutic Areas

90+

Countries

8000+

Sites

Power your RWD trials with oomnia

Streamline real-world data studies using our unified trial software

Intelligent Data Oversight

Our clinical data managers focus on collecting, extracting, and reviewing only the most important data points. This helps reduce unnecessary data and manual work. Your team can focus on the evidence that really matters and move faster with fewer distractions.

Customizable RWD/RWE Strategies

Real-world data trials need flexible approaches, and we support them all. Use simple or double data entry, connect EHRs directly to oomnia, or work with eSource solutions. Our system and team adapt to your needs and ensure you get the right setup for your trial.

Seamless EHR Integration and Real-Time Insights

oomnia integrates with EHR systems via HL7 and FHIR, enabling structured, automated data transfer from routine care into your study. This ensures real-time availability and seamless support for both digital and hybrid workflows.

Empowering Teams with Professional Support

From the first risk assessment through to ongoing RWD/RWE operations, we help define data sources, assess regulatory requirements, and set up fit-for-purpose workflows. With us, you gain practical tools and expert guidance.

Eager to Explore Tailored Services?

Discover how our clinical trial services can support your trial research. We combine hands-on expertise with smart tools to help you run faster, smoother, and more compliant trials.

Tell Us About Your Trial

Flexibility Across All Clinical Study Designs

Whether you're running an innovative medical device study or a decentralized trial, oomnia is built to support it. Our flexible platform adjusts to your needs, empowering teams to collaborate efficiently, no matter the trial design.

Decentralized Trials

Explore All oomnia Features

oomnia offers eight essential, fully interoperable tools for easier clinical study management. Integrate seamlessly with existing systems, use only what you need, and capture real-time data from multiple digital sources.

EDC

RTSM

eTMF

CTMS

eConsent

ePro

eCOA

eSource

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