Wemedoo AG empowers biopharma, medtech, CROs, and academic teams to run faster, smarter, and compliant clinical trials with one unified system. Our solution combines real-time insights, clinical data management, analytics, and regulatory
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compliance to reduce costs, accelerate timelines, and simplify trial complexity.
Wemedoo’s oomnia system unifies powerful tools including CTMS, EDC, eTMF, ePRO, eCOA, eConsent, eSource, and RTSM, enabling end-to-end oversight and seamless collaboration across the clinical trial lifecycle.
