oomnia by Wemedoo is the first true all-in-one clinical trial solution, unifying clinical research and clinical practice within a single platform. It integrates all essential clinical trial tools—including EDC, RTSM, CTMS, eTMF, ePRO, eCOA, eConsent, and eSource—into one seamless system. Designed for hospitals, research organizations, and clinical trial sponsors, Oomnia improves efficiency, reduces errors, and ensures regulatory compliance while enabling real-time oversight and collaboration across clinical workflows.

Key benefits include up to 80% time savings, improved data quality, enhanced patient care, and a foundation for future AI-driven healthcare modules.

What are the main features of Oomnia?

Unified clinical trial platform

Oomnia consolidates all core trial components into one system:

• EDC (Electronic Data Capture) for accurate, real-time data collection

• RTSM (Randomization and Trial Supply Management) to ensure smooth trial operations

• CTMS (Clinical Trial Management System) to track study progress and milestones

• eTMF (Electronic Trial Master File) for centralized, compliant documentation

• ePRO/eCOA (Patient-Reported and Clinical Outcome Assessments) to gather patient data digitally

• eConsent and eSource for streamlined patient enrollment and source data collection

Real-time collaboration and data interoperability

Oomnia ensures full clinical data interoperability, connecting seamlessly with any EHR or existing clinical system:

• Instant access to trial and clinical practice data

• Real-time collaboration between investigators, coordinators, and sponsors

• Integration without programming or custom development

• Supports trial-agnostic workflows adaptable to specific study requirements

Workflow automation and efficiency

Oomnia reduces manual work and errors, significantly accelerating trial processes:

• Streamlined data entry, validation, and reporting

• Automation of routine tasks, reducing administrative overhead

• Continuous oversight of trial and clinical workflows

• Up to 80% time savings on repetitive processes

Clinical data quality and regulatory compliance

Oomnia safeguards data integrity and compliance:

• Compliance with industry standards and regulations

• Audit-ready records with full traceability

• Standardized processes to improve patient care and trial outcomes

Foundation for future AI integration

Oomnia’s clinical core is AI-ready, ensuring compatibility with next-generation healthcare modules:

• Structured, high-quality datasets

• Scalable architecture for AI-driven insights

• Continuous support for innovation in clinical research

Why choose Oomnia?

• All-in-one platform: Combines research and clinical practice tools in a single system

• Trial-agnostic and adaptable: Works with any EHR and flexible workflows

• Time and labor savings: Up to 80% reduction in manual tasks

• Real-time oversight: Full visibility across trials and clinical operations

• AI-ready clinical core: Future-proof solution for emerging healthcare technologies

Oomnia streamlines clinical trial management, reduces operational complexity, and enhances patient outcomes by unifying research and practice in one scalable, AI-ready platform.