The core activity of Wemedoo AG is the development and provision of software solutions for clinical research and data management, particularly in the field of clinical trials and medical research. The solutions include, among others, eSource, RTSM, eTMF, ePro, eCOA, eConsent and CTMS tools, which aim to improve the efficiency and quality of clinical trials.
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Industry:Software Development
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Unified clinical trial software for EDC, CTMS, RTSM, eTMF, ePRO, eSource, eConsent and eCOA, with real-time data, audit trails and compliance features.
Professional Services for Clinical Trials
Professional services for study design, protocol development and medical writing, clinical data management, and biostatistics and statistical programming.
Electronic Data Capture (oomnia EDC)
Electronic capture of clinical data with configurable eCRFs, real-time validation, data integrity controls and support for complex study designs.
Clinical Trial Management System (oomnia CTMS)
Central trial management with real-time oversight, site monitoring, financial milestones, team coordination and dashboards for operational control.
Electronic Trial Master File (oomnia eTMF)
Central electronic trial files for document management, inspection readiness, audit support and traceable storage of clinical documents.
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