eCOA All Clinical Outcomes in One Place
oomnia eCOA captures every perspective, securely, in real time, and fully synced with your trial.
Superior patient engagement
eCOA oomnia eCOA captures every perspective, securely, in real time, and fully synced with your trial.
Deliver a user-friendly interface that makes data entry a breeze, driving higher compliance and active participant involvement.
Enable true BYOD support for smartphones, tablets, and computers – ensuring participants can contribute data anytime, anywhere with minimal setup.
Use advanced analytics and real-time reporting to drive informed decisions and elevate trial accuracy.
Experience fast data integration that empowers rapid decision-making and accelerates study timelines.
Empower your participants with a user-friendly interface that boosts engagement and simplifies data entry.
Cut manual tasks with automated data management and built-in BYOD support – saving time and reducing expenses.
Immediate validation checks catch discrepancies instantly, reducing mistakes and enhancing data quality.
Capture every insight – from structured forms to unstructured feedback – in one powerful platform.
Customize forms and IoT inputs to perfectly match your study’s unique needs.
Automatically enforce industry standards for uniform, ready-to-analyze data.
Avg. Completion Time
Data Entries Processed Daily
Patient Compliance
Devices Supported
Inspired by the Latin Word omnia, Meaning 'All Things',
We Created oomnia.
A single, unified system that brings together every part of a clinical trial, from planning to global compliance.
EDC, RTSM, eTMF and CTMS, eSource, ePRO, eCOA and eConsent are integrative parts of one and the same ecosystem supporting multiple trials on a single instance.
Choose the modules and features that work for you and customize everything to fit your workflow.
Optimized Trial Operations
Smart, Automated Notifications
Get real-time alerts and scheduled reminders that keep your study on track.
Transparent Audit Trail Insights
Gain complete visibility with detailed logs that ensure full traceability.
Flexible Trial Design Support
Adapt effortlessly to diverse protocols, managing both subjective outcomes and objective assessments.
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
Integrate forms, notes, biomarkers, sensor data, and adaptive surveys.
Boost retention with an intuitive, mobile-friendly design and interactive assessments
Take advantage of real-time analytics, automated alerts, and strict validation for quick decisions.
Support any trial design while evolving with all of your data needs.
Customize capture tools and maintain robust audit trails for flawless data integrity
Boost compliance and secure timely data capture with proactive notifications
Read more about the experiences from those who have partnered with us
All jobs, both large and small, are performed with the same dedication to quality, detail, innovative thinking, and rigor. It is always a pleasure to work with the Wemedoo team.
Georg Mathis, PhD
CEO Appletree CI Group AG
Wemedoo embodies all the traits desired in a partner in the clinical trial industry – expertise, innovation, reliability, compliance, and attention to detail.
Martina Diminic Smetisko, DMD
Managing Director at Marti Farm Ltd
Their dedication to, and support of, our projects has resulted in clear quality deliverables. They are always there to answer any questions with expertise in a timely manner. I am looking forward to our next project together.
Volodymyr Stus, MD
Biopharmaceutics and Clinical Research Department Manager at Polpharma SA
Our Proof of Quality
We are ISO 9001 and ISO 27001 certified. Our commitment to robust information security & superior quality management is at the core of our innovative solutions, ensuring reliable & efficient trial management for our clients.
THANK YOU FOR YOUR INTEREST
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Get the answers you need about oomnia eCOA.
oomnia eCOA is an electronic Clinical Outcome Assessment platform that enables participants and site staff to report data directly using electronic devices. It improves data collection by enhancing accuracy, speed, and engagement in clinical trials.
Key features include real-time data integration with our EDC, RTSM, and CTMS, a user-friendly interface, enhanced participant engagement, streamlined communication, simplified document management, and compliance with regulatory standards.
Real-time data integration allows for immediate updating and centralization of trial data within our oomnia EDC and CTMS system, significantly improving management, efficiency, and decision making, while reducing costs and human resources for clinical trials.
Yes, oomnia eCOA is designed with an intuitive user interface and includes a participant landing page with clear guidelines, making it accessible and easy to use for individuals with varying levels of digital literacy.
oomnia eCOA maintains high standards for compliance and inspection readiness through its real-time data integration, comprehensive data management system, audit trails, and adherence to regulatory requirements.
The platform enhances participant engagement by enabling direct, real-time reporting of data through familiar electronic devices, fostering a more involved and responsive trial experience. Participants can use their own devices thereby breaking down barriers for their participation.
Yes, oomnia eCOA provides comprehensive user support throughout clinical trials, including technical assistance and guidance on best practices for using the platform effectively.
In order to book a demo call with an oomnia expert, simply press the button below, select a date in the booking tool and fill in all necessary information. After that, we will send you an invitation.
