🇨🇭 Swiss Data Privacy & Precision

Every Clinical Trial Type. One Unified Platform.

Interventional, Observational, Decentralized & Real-World Studies

Whether you're running a Phase I first-in-human study, a multi-regional pivotal trial, a decentralized hybrid study, or a real-world evidence program, oomnia adapts to your protocol — not the other way around. Our unified platform supports every trial type across all therapeutic areas with full regulatory compliance.

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ISO 27001 SOC 2 FDA 21 CFR Part 11 GDPR & HIPAA

Handling Multiple Types of Clinical Trials

Explore Our Flexible Solutions for a Variety of Trial Types

oomnia supports a variety of trial types, ensuring flexibility and scalability for different clinical research demands. Whether you are conducting a complex decentralized trial, gathering real-world data, or leading an innovative medical device trial, oomnia offers the tools and support to enhance every stage of your research. Discover how our software brings efficiency and precision to your individual clinical research needs. Explore the full scope of trials supported by oomnia, where every research challenge finds its solution.

Medical Device Trials

Real-World Data Trials

Decentralized Trials

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Medical Device Trials

Optimize Every Phase of Your Device‘s Lifecycle

Medical device trials require precise data management and adherence to strict regulations. With oomnia, you can easily manage your trials through one streamlined platform, offering real-time insights, monitoring, and regulatory compliance features. Stay ahead with comprehensive data management, automated compliant datasets customized reporting, and full visibility across all trial stages.

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Real-World Data Trials

Enhance Your Trials to Obtain Real-World Evidence

oomnia supports real-world data trials by integrating EHRs and other healthcare data sources, ensuring seamless data collection and analysis. With custom validated real-world data, real-time insights, and regulatory compliance, your team can make informed decisions based on accurate and up-to-date information. Our scalable platform ensures that your RWD trials stay efficient, compliant, and secure.

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Decentralized Trials

Gather Data from Patients, Clinicians & Caregivers

Decentralized clinical trials have never been easier to manage. With our powerful tools, you can engage participants from anywhere, while maintaining oversight of patient-reported outcomes, data quality, and trial progress. Seamlessly capture eConsent, ePRO, and real-time data without delays, ensuring your trial stays on track while reducing patient burden.

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oomnia - Meeting Industry Standards

Our unified clinical trial software is designed with compliance at its core, meeting critical industry standards. Our commitment to these regulations ensures that your clinical trials are not only efficient but also adhere to the highest levels of data integrity, privacy, and ethical conduct.

21 CFR
PART11

compliant

HIPAA

compliant

GDPR

compliant

ICH GCP

compliant

SWISS DATA PRIVACY LAW

compliant

FAIR ALCOA+

compliant

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

Every Clinical Trial Type. One Unified Platform.

Interventional, Observational, Decentralized & Real-World Studies

Medical Device Trials

Real-World Data Trials

Decentralized Trials

Medical Device Trials

Optimize Every Phase of Your Device‘s Lifecycle

Real-World Data Trials

Enhance Your Trials to Obtain Real-World Evidence

Decentralized Trials

Gather Data from Patients, Clinicians & Caregivers

Trusted by Global Clinical Research Teams

Trusted by Global Clinical
Research Teams