eSource eSource That WOrks in Real-Time
Access clinical data directly at the source. Structured, validated, and always up to date.
Superior patient engagement
eSource Access clinical data directly at the source. Structured, validated, and always up to date.
Avoid Entering the Same Data More than Once. Clinical Data is Captured Directly Where Care Happens.
All stakeholders work with the same data in real time. This improves quality, reduces delays and increases transparency. The eSource supports hospitals, research sites and remote trials. The data is ready to use, easy to audit and always follows the protocol.
Wemedoo brings deep clinical knowledge into the system. Its core strength is the structuring and standardization of clinical data. This makes the data easier to work with, faster to analyze and ready for reuse.
Connect data from different digital sources in real time. Clinical data is captured at the moment it is created and flows directly into your trial database with full accuracy.
Create custom data forms with ease. The design tool is simple to use and ensures all collected data matches your clinical protocol and is fully validated.
Capture trial data with smart forms that match your protocol and adapt to any standard.
View live reports that bring together all data streams for full trial visibility.
Monitor entries and compliance in real time to ensure data quality and protocol alignment.
Avoid mistakes with direct input, automated checks and real-time synchronization.
Launch trials quickly using pre-built templates and seamless system integration.
Cut manual work with automated data flows and digital source documentation.
Seamless Data. Smarter Workflows.
Clinical Data Accuracy
Capture clinical data exactly where it is created. No more manual transcription, no more back-and-forth reconciliation between systems.
With oomnia, direct data entry replaces source verification and enables smooth protocol translation into real-world clinical workflows. It also supports central readings and advanced use cases, from visit notes to lab assessments.
Smart Integration Capabilities
Connect smoothly with hospital systems using HL7 and FHIR standards. Our flexible data model speaks the language of clinical informatics and adapts to the terminology used at each site.
The system is built on Common Data Elements. This allows reuse of validated data forms and speeds up database setup and review.
Flexible Data Streams
Collect all types of clinical data, from vital signs to voice notes and lab reports. The system accepts different formats and connects with wearables and home-monitoring devices using an IoT-ready engine.
This makes oomnia ready for both site-based and decentralized trials.
Faster Trial Setup Up To
Real-Time Trial Oversight
Client Retention
Ensure accurate entries with built-in consistency checks that catch errors early and reduce the need for corrections.
Your data stays aligned at all times thanks to live updates across every connected system.
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.
Protect sensitive data with 21 CFR Part 11–compliant encryption, secure login protocols, and role-based access. All actions are logged and traceable for full audit readiness.
Connect sponsors, sites, and CROs through secure, shared workspaces. Real-time access to the same data set ensures aligned decisions, fewer back-and-forths, and faster resolution of queries.
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
Looking to explore more? Get our eConsent flyer for more details.
