oomnia CTMS

oomnia Clinical Trial Management System (CTMS) by Wemedoo centralizes and automates the management of clinical trials from initial planning through final reporting. It integrates key trial components, including participant data, site selection, budgeting, and document management. Designed as part of a unified clinical research platform, it supports data integration across modules and maintains alignment with data protection standards such as GDPR and HIPAA. Users such as clinical data managers, trial directors, and research associates access real-time data on study progress, adverse events, protocol deviations, and enrollment milestones. By consolidating and updating information from eCRFs, RTSM, eTMF, ePRO, and eCOA tools, CTMS reduces manual tasks, input errors, and delays, helping reduce operational costs and cycle times. The software allows tracking of expenses, participant visits, site activation status, staff training progress, and delegation records.