Simplify study logistics and drive faster, smarter trial outcomes
oomnia RTSM is part of one unified system. No switching, no delays, no gaps.
Manage your study from one unified hub that combines EDC and RTSM. No switching between separate systems. With every function under one roof, you save time, reduce errors, and keep your trial on track.
Randomize participants, verify IMP availability, assign the correct kit and allocate the study arm at a click of a button. All simultaneously and tracked in real time.
Randomize directly from the eCRF. With a single click.
We support various standard randomization approaches and algorithms. Our flexibility allows us to develop and validate any non-standard approach.
Want to randomize a device or an image reader? Our data model is flexible by design. It supports randomization of any object, not just participants.
Our unified database model allows direct communication between EDC and RTSM. Therefore, reconciliation is unnecessary, and manual work is eliminated.
With EDC and RTSM data within one database, you can control any aspect of clinical operations in real time. oomnia allows you to focus on critical elements and prevent protocol deviations.
With EDC and RTSM data within one database, you can control any aspect of clinical operations in real time. oomnia allows you to focus on critical elements and prevent protocol deviationsoomnia RTMS takes care of drug supply. oomnia power automation tools support you from organizational and oversight perspectives of drug supply.
oomnia RTSM for Smart Supply Logistics
Smart Alerts & Notifications
Receive instant notifications when inventory drops or nears expiry, keeping you in complete control.
Dynamic Expiry Protection
Automatically notify study stuff about soon-to-expire IMPs, ensuring patient safety and compliance. Block delivery of expired investigational products.
Instant, Accurate Kit Assignment
Eliminate manual checks with automated kit allocation that guarantees perfect treatment assignments every time.
Cost Reduction Up Tp
Increase in Operational Efficiency
Approx. Data Quality
oomnia allows highly specific role-based permissions, ensuring that users have exact control over data and workflows. From data management to CRF setup and validation, all access levels are managed seamlessly.
SAVE UP TO 75% OF NAVIGATION TIMEExperience the freedom of a drag-and-drop builder that lets you craft robust eCRF forms without writing a single line of code. No IT support required, just pure efficiency.
0%PROGRAMMING REQUIREDoomnia significantly reduces manual data cleaning, unnecessary queries, and reconciliation work. Users report dramatic reductions in time spent resolving queries and managing SDV.
REDUCE UP TO 66%OF MANUAL QUERIES
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.
oomnia RTSM Features Improve Your Clinical Research
Assign treatment groups with absolute precision
Control trial resources for smooth supply flow
Unify study data for actionable, instant insights
Guarantee full protocol adherence
Convert reports for fast analysis and seamless stakeholder collaboration