Electronic Data Capture (EDC) Software

Real-Time Oversight for Clinical Data Managers and Sponsors

Eliminate manual data reconciliation, resolve discrepancies instantly, and accelerate database lock with an EDC built for complex, global trials.

oomnia EDC real-time clinical trial reporting dashboard

Powerful Dashboards for Real-Time Reporting

Generate custom reports, dashboards and statistical analyses directly within the system. All data is analysis-ready at any time and you decide what and how to present your data.

Intuitive User Interface

Positive user experience, intuitive design and powerful no-code user interface allows efficient workflow and productive collaboration.

Why Our Clients Love oomnia EDC

Advanced Participants Dashboards

Get a clear, detailed view of every participants' journey. Track data entry, query resolution, SDV progress or study milestones in real-time.

Usability & Reduced Cognitive Load

Role-specific views show only what is needed. It streamlines tasks, reduces errors, and speeds up work.

Automated Notifications

Instant alerts for query responses, protocol deviations, and milestone deadlines gives you a complete oversight across trials.

Built-in Business Analytics

Data flows directly into built-in analytics. It is always structured, always analysis-ready, no extra steps required.

Built For Clarity

Role-based access and intuitive navigation, boost confidence across teams.

Smooth RTSM Integration

Instant randomization of IP kits with automated tracking within the RTSM.

Accelerate Your Clinical Data Lifecycle

Drag-and-drop eCRF form designer for clinical trials

No-Code eCRF Design & Mid-Study Updates

CRFs are created without programming. The intuitive, drag-and-drop interface, built-in templates, field validations, and logic rules simplify the setup process and ensure compliance from the start.

Automated query resolution and task routing in oomnia EDC

Automated Query Management & Edit Checks

Tasks are automatically routed to the right users. Edit checks run in real time. Discrepancies are flagged instantly. Sites respond faster, monitors spend less time reviewing, and rework is reduced. Everyone sees only what they need to act.

CDISC and SDTM compliant data export dashboard

Faster Data Submission & Regulatory Readiness

Data is exportable in SDTM format and fully CDISC-compliant. No need for separate CDASH programming. This accelerates regulatory submission and saves months of manual preparation.

Up To 83% Faster Trial Setup

100% Real-Time Trial Oversight

100% Client Retention

Clients using oomnia EDC report up to an 83% faster clinical trial setup and a 66% reduction in manual queries compared to traditional EDC systems.

Case Studies, Our Proof of Expertise

Ophthalmology Medical Device & Drug Study

Streamlined Study & eCRF Implementation: Managed a complex study with 5000+ CRF questions and dynamic eCRF features that reduced manual queries by 66%.
Rapid Execution & Training: Completed design, implementation, UAT, and site training in just 9 weeks, ensuring a smooth go-live.
Accelerated Study Timelines: Achieved database lock within 2 weeks after the last patient’s visit, significantly speeding up the study.

Medical Device Real-World Evidence Study

Holistic Study Design: Integrated retrospective data collection and prospective ePRO arms, with expert protocol development.
Seamless Digital Integration: Leveraged oomnia EDC, eConsent, and ePRO to streamline data collection, consent, and patient engagement.
Automated Workflows & Unified Data: Implemented dynamic eCRF automation and real-time consent tracking with integrated data management for flawless protocol oversight.

Automated Oversight for a Phase IV Pediatric Study

Comprehensive & Real-Time PD Tracking: Developed a robust log capturing all protocol deviations in detail, with real-time reports by country, site, and participant.
Automated Role-Based Alerts: Implemented automatic email notifications that alert designated roles for timely review and approval.
Streamlined Data Entry & Resolution: Dynamic behaviors reduce redundant questions and dramatically cut the time needed to track, review, and resolve deviations.

oomnia EDC Sets a New Standard for CROs and Sponsors

Granular User Access Control

oomnia allows role-based permissions across all trials and oomnia modules. From data management to CRF setup and validation, all access levels are managed seamlessly with a single sign-on.

SAVE UP TO 75% OF NAVIGATION TIME

Flexible eCRF Form Designer

The system is based on intuitive drag-and-drop functionality, supporting the easy setup of highly complex configurations without programming.

0%PROGRAMMING REQUIRED

Reduced Query Resolution & Time

oomnia significantly reduces manual data cleaning, significant queries, and reconciliation work. Users report significant reductions in time spent resolving queries and managing SDV.

REDUCE UP TO 66%OF MANUAL QUERIES

Common Questions

Frequently Asked Questions

What is EDC software in clinical trials?

EDC (Electronic Data Capture) software is a digital system used to collect, manage, and validate clinical trial data electronically. Wemedoo's oomnia EDC software replaces paper-based case report forms (CRFs) with electronic CRFs (eCRFs), enabling real-time data entry, automated validation, and faster regulatory submissions.

What are the benefits of oomnia EDC software?

oomnia EDC software offers real-time dashboards for instant reporting, an intuitive drag-and-drop eCRF designer, automated query management, built-in business analytics, granular user access control, and seamless integration with RTSM, eTMF, and other clinical trial tools within one unified system.

How does oomnia EDC compare to other EDC systems?

Unlike standalone EDC systems that require separate integrations, oomnia EDC is natively unified with CTMS, eTMF, RTSM, ePRO, and eConsent. This eliminates data reconciliation, reduces study setup time, and provides a single source of truth for all clinical trial data.

Is oomnia EDC software compliant with 21 CFR Part 11?

Yes, oomnia EDC software is fully compliant with 21 CFR Part 11, HIPAA, GDPR, and ICH GCP requirements. It includes complete audit trails, electronic signatures, role-based access control, and data encryption to ensure regulatory readiness at all times.

How fast can a study be set up using oomnia EDC?

oomnia EDC enables faster study setup through its drag-and-drop eCRF form designer, reusable templates, and automated validation rules. Studies can be configured and validated significantly faster compared to traditional EDC systems, reducing time-to-first-patient.

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.

Electronic Data Capture (EDC) Software for Clinical Trials

The No-Code EDC Built to Accelerate Complex Clinical Trials

Real-Time Oversight for Clinical Data Managers and Sponsors

Powerful Dashboards for Real-Time Reporting

Intuitive User Interface

Why Our Clients Love oomnia EDC

Advanced Participants Dashboards

Usability & Reduced Cognitive Load

Automated Notifications

Built-in Business Analytics

Built For Clarity

Smooth RTSM Integration

Accelerate Your Clinical Data Lifecycle

No-Code eCRF Design & Mid-Study Updates

Automated Query Management & Edit Checks

Faster Data Submission & Regulatory Readiness

Case Studies, Our Proof of Expertise

Ophthalmology Medical Device & Drug Study

Medical Device Real-World Evidence Study

Automated Oversight for a Phase IV Pediatric Study

oomnia EDC Sets a New Standard for CROs and Sponsors

Granular User Access Control

Flexible eCRF Form Designer

Reduced Query Resolution & Time

Frequently Asked Questions

What is EDC software in clinical trials?

What are the benefits of oomnia EDC software?

How does oomnia EDC compare to other EDC systems?

Is oomnia EDC software compliant with 21 CFR Part 11?

How fast can a study be set up using oomnia EDC?

Trusted by Global Clinical Research Teams

Real-Time Analytics

Unified SaaS-Solution

Full Interoperability

Swift Validation Process

Adaptive Flexibility

Enhanced Usability

Easy Learning Curve

Instant Collaboration

Exceptional Services

Reading Material

Download EDC Brochure

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Trusted by Global Clinical
Research Teams