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DirectoryIT & CommunicationSoftware DevelopmentSteinhausenWemedoo AG
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Wemedoo AG

Summary

About the company

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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Unified Clinical Trial Software (oomnia Platform)
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.
Randomization and Trial Supply Management (oomnia RTSM)
Automated randomization and investigational product supply management for global sites, with traceable allocation and supply oversight.
Electronic Patient-Reported Outcomes (oomnia ePRO)
Digital capture of patient-reported outcomes in real time, with user-friendly data submission and support for participant compliance.
Electronic Clinical Outcome Assessments (oomnia eCOA)
Standardized electronic capture of clinical assessments with consistent data collection across global trial sites.
eSource Data Capture (oomnia eSource)
Direct capture of clinical information at the point of care, reducing transcription errors, speeding data availability and simplifying source data verification.
Electronic Informed Consent (oomnia eConsent)
Digital informed-consent workflows with interactive capture, compliance support and cross-device use for participants.
Trial Design and Medical Writing
Support for study design, protocol development, informed consent forms, lay summaries, clinical study reports and submission documents.
Biostatistics and Statistical Programming
Biostatistical analysis and statistical programming for study design, analysis and regulatory submission, with CDISC-compliant SDTM and ADaM datasets.
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Location

Sumpfstrasse 24
6312 Steinhausen

At a glance

Legal form
Corporation
UID
CHE-290.176.074
Founded
2020 · 6 years
Last commercial register change
February 3, 2026
Employees
11 to 20

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