Clinical Trial Software
One unified clinical platform for every clinical trial type
oomnia is a clinical trial software platform designed to support interventional, observational, decentralized, and real-world studies within a single, unified system.
Clinical Trial Types
Supporting multiple clinical trial types within one platform
oomnia provides the flexibility and scalability teams need across different research models and adapts to the demands of each trial type.
Real world data trials
Collect structured, validated real-world data within a unified system, supporting regulatory-ready insights.
Decentralized trials
Enable remote participation and data capture while maintaining centralized oversight, compliance, and data consistency.
Phase I – Phase IV trials
Designed to support Phase I through Phase IV trials, from first-in-human studies to post-approval research.
Who We Work With
Built for every clinical research team
oomnia is designed to meet the needs of diverse clinical research teams, adapting to different scales, study models, and operational realities. From global sponsors to resource-limited teams, oomnia provides the structure, flexibility, and visibility required to run studies efficiently.
Explore how oomnia supports different organizationsTrusted partners
Global network of partners
oomnia Platform
Unified clinical workflows across all trial types
Bringing clinical trial tools together in one system to support diverse teams and research environments
Electronic Data Capture (EDC) Software
Streamline clinical data collection with our intelligent, compliant EDC system. Build complex trial designs quickly, reduce data entry errors, and ensure absolute data integrity.
Clinical Trial Management System (CTMS)
Gain complete, real-time oversight of your trial operations. Centralize site monitoring, track financial milestones, and manage your clinical teams from one unified dashboard.
Electronic Trial Master File (eTMF)
Maintain constant inspection readiness and compliance. Streamline your clinical document management with a secure, centralized repository that simplifies audits and tracking.
Randomization & Trial Supply Management (RTSM)
Automate complex patient randomization and optimize your clinical supply chain. Ensure the right treatments reach the right global sites exactly when they are needed.
Electronic Informed Consent (eConsent)
Improve patient comprehension and trial retention with an interactive, fully compliant digital consent experience that works seamlessly across devices.
Electronic Patient-Reported Outcomes (ePRO)
Capture high-quality, real-time data directly from patients. Our user-friendly ePRO boosts patient engagement and compliance by making data submission effortless.
Electronic Clinical Outcome Assessments (eCOA)
Standardize your clinical assessments to ensure high-fidelity data collection. Eliminate paper-based inconsistencies and capture reliable outcome data across all global trial sites.
eSource Data Capture
Accelerate data availability by capturing clinical information directly at the point of care. Eliminate manual transcription errors and streamline source data verification (SDV).
Therapeutic Areas
Supporting trial types across all therapeutic areas
oomnia is built to support clinical research across different trial designs and therapeutic areas within a single platform, eliminating the need for separate systems or indication specific configurations. With a shared data foundation and configurable workflows, research teams can run a wide range of trial types across multiple therapeutic domains while maintaining consistent data standards, streamlined operations, and centralized oversight.
Explore how oomnia supports research across therapeutic areasGet Started
See how one platform supports every trial type
Deliver flexibility and consistency across interventional, decentralized, and real-world studies with oomnia
Talk to our team