About Wemedoo
Wemedoo AG is a Swiss health-tech company and global team of clinical data specialists. We developed oomnia, a unified Clinical Research Information System (CRIS), dedicated to breaking down data silos, accelerating time-to-market, and improving patient outcomes worldwide.
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Headquartered in Switzerland
Rooted in Swiss precision and quality, our experts help research organizations globally eliminate fragmented workflows. We bridge the gap between software and scientific execution, ensuring your trials are powered by clean, connected, and fully compliant real-time data.
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What We Do
We combine a unified clinical research platform with specialized operational expertise to help teams move from protocol to submission with fewer tools, fewer handoffs, and better data.
One validated system connecting all clinical trial data — no silos, no reconciliation overhead.
Intelligent tools that surface anomalies, accelerate review cycles, and improve data quality at scale.
Live dashboards and cross-functional visibility across every study, site, and data point.
End-to-end CDM from database design and edit check programming through to database lock.
Statistical analysis plans, CDISC-compliant datasets, and submission-ready documentation.
Protocol development, regulatory documentation, and data strategy aligned with your endpoints.
Our Platform
A secure clinical trial software that centralizes clinical data and operations into one unified, AI-powered research ecosystem. Unlike traditional eClinical systems, it is built on a single data model that ensures consistency and real-time visibility across the entire trial.
Explore more about oomniaOur Services
Expert support across critical functions
Explore all servicesWho We Serve
From global pharma to academic research sites, our unified platform adapts to how your team works.
End-to-end trial data management from Phase I through post-market surveillance in a single, validated system.
Multi-sponsor trial management with centralized oversight, scalable across therapeutic areas and geographies.
Enterprise-grade eClinical tools purpose-built for investigator-initiated trials and institutional research.
Integrated workflows for device trials and digital therapeutics with full regulatory traceability.
eSource, eConsent, and real-time data capture designed for the realities of day-to-day site operations.
Clinical-grade data management bringing regulatory rigor to consumer health and wellness research.
Our Leadership
Chief Executive Officer
MSc in Business Administration from the University of St. Gallen. Drives Wemedoo's strategy to make clinical research more efficient and accessible worldwide.
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Founder and Chief Product Officer
Physician and radiation oncologist with 15+ years at Switzerland's largest university hospital. Active contributor to mCODE, HL7/FHIR, CDISC, and DIA Europe working groups.
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Chief Customer Officer
PhD in molecular medicine with specialization in neuroscience (University of Alberta). Expert in biostatistics, CDISC data standards, and clinical data operations.
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Chief Operating Officer
MA in Strategy and International Management from the University of St. Gallen. Brings deep life sciences consulting experience across the pharmaceutical value chain.
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Director of Quality Management
Master of Pharmacy from the University of Belgrade. Architect of Wemedoo's ISO 9001 and ISO 27001 certified quality system with 70+ SOPs.
Connect on LinkedInLatest Updates
Sep 2025
Our founder discusses Wemedoo's mission to unify fragmented healthcare systems through oomnia — covering standardized data, ethical AI, no-code flexibility, and patient-centric solutions.
Jul 2025
Integration of mediri's mTRIAL platform with oomnia gives research teams real-time access to imaging analysis, browser-based scan review, and protocol-driven workflows.
Mar 2025
Wemedoo's mission to fix clinical research: one database, single sign-on, real-time oversight, drag-and-drop setup, and full compliance — all in one unified system.
Jul 2024
oomnia changes the game by unifying all essential functionalities for a successful clinical trial into one seamless system with a single login and interface.
Feb 2024
Our clinical data management and biometrics team, led by Urosh Vilimanovich, was recognized for Team Excellence in the Management of Clinical Data.
Dec 2023
From planning to execution, our innovative platform streamlines every aspect of clinical trial workflow, ensuring excellence at every step.
Aug 2023
oomnia connects tools across clinical trial lifecycles, offering real-time insights and streamlining complex trial processes without specialized software overhead.
Jul 2023
At Wemedoo we believe interoperability is foundational to modern clinical research — connecting data, systems, and teams across the entire study lifecycle.
Jul 2023
How implementing RTSM solutions automates inventory and supply chain processes within clinical research, reducing manual overhead and improving trial efficiency.
Jan 2024
Setting ambitious goals for 2024 — committing to explore new frontiers and build on our legacy of excellence in clinical data management.
Testimonials
Wemedoo's technology, expertise, and intimate engagement with our team in the development of the EDC, site/patient interface, and metric capabilities are unique, one-size-fits-all and they adapt to the needs of the sponsor, sites…
James Kuras
Vice President of Clinical Affairs and Operations at Centinel Spine
Wemedoo's cross-functional, integrated teams capture EDC set-up, go-live, data capture, data cleaning, and finally data analysis in a globally compliant fashion supporting trials in different geographies including the US…
Friedrich Asmus
Former Chief Medical Officer at OXULAR
All jobs, both large and small, are performed with the same dedication to quality, detail, innovative thinking, and rigor. It is always a pleasure to work with the Wemedoo team.
Georg Mathis, PhD
CEO at Appletree CI Group AG
Wemedoo embodies all the traits desired in a partner in the clinical trial industry – expertise, innovation, reliability, compliance, and attention to detail.
Martina Diminic Smetisko, DMD
Managing Director at Marti Farm Ltd
Their dedication to, and support of, our projects has resulted in clear quality deliverables. They are always there to answer any questions with expertise in a timely manner. I am looking forward to our next project together.
Volodymyr Stus, MD
Biopharmaceutics and Clinical Research Department Manager at Polpharma SA
Envisioning Tomorrow’s Clinical Trials
MEET AN EXPERTOur People
Our professional team stands as one of our most invaluable assets, driving innovation, expertise, and dedication to excellence.
Our Vision
At the heart of our company lies innovation, customer focus, and result orientation, driving us to pioneer new solutions and tangible results.
Our Journey
Our journey is fueled by a relentless commitment to progress, collaboration, and excellence, guiding us to enhancing healthcare efficiency and accessibility.
Sustainability
We are deeply committed to sustainability, innovatively enhancing our operations to foster a healthier planet for future generations.
Unified Healthcare
We unify healthcare through innovative solutions, enhancing system integrations and efficiency to improve patient care.
Our Products
With an innovative approach in mind, we challenge norms, drive transformative change within our industry and pioneer new solutions.
We embrace a culture of innovation & creativity to push the boundaries of technology.
We combine state of the art technology with personal expertise & dedication to deliver the best results to our customers.
We stay true to our word, pay attention to details, and never compromise quality in anything we do & deliver.
oomnia - Meeting Industry Standards
Our unified clinical trial software is designed with compliance at its core, meeting critical industry standards. Our commitment to these regulations ensures that your clinical trials are not only efficient but also adhere to the highest levels of data integrity, privacy, and ethical conduct.
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Common Questions
Wemedoo provides a Clinical Research Information System (CRIS) that helps research teams run smarter, faster, and fully connected clinical trials. Through one unified system, oomnia, Wemedoo brings together all core clinical trial processes into a single, structured environment. oomnia offers eight essential clinical trial tools: Electronic Data Capture (EDC), electronic Clinical Outcome Assessment (eCOA), electronic Patient-Reported Outcomes (ePRO), Clinical Trial Management System (CTMS), electronic Informed Consent (eConsent), electronic Source Data (eSource), Randomization and Trial Supply Management (RTSM), and electronic Trial Master File (eTMF) in one system to advance trials, improve data quality, and reduce costs.
Wemedoo AG is a Swiss-based clinical research software company providing AI-powered, data management solutions centered around a unified clinical research information system. Its system oomnia supports regulated clinical research by enabling unified data management, operational oversight, and compliance across the full clinical trial lifecycle.
Wemedoo comes from the idea of "we do medicine." It reflects the belief that healthcare is a shared effort and that progress is achieved when people collaborate across disciplines.
Wemedoo stands for collaboration and action. We unify clinical research and clinical practice through structured, reusable clinical data. It reflects the idea that better medicine is something we build together across disciplines, institutions, and borders.
Unlike traditional clinical trial software vendors that offer fragmented, standalone tools, Wemedoo delivers a fully unified Clinical Research Information System. All modules within oomnia operate on a single database and user interface. This unified architecture eliminates manual data reconciliation and provides real-time visibility across clinical operations.
oomnia is Wemedoo's Clinical Research Information System, designed as a single data environment for clinical trials. It brings together data capture, trial operations, documentation, and real-time oversight in one structured and interoperable system.
Wemedoo is ISO 9001 and ISO 27001 certified and aligns with major clinical research and data privacy standards, including ICH GCP, 21 CFR Part 11, HIPAA, GDPR, Swiss Data Privacy Law, and ALCOA+ data integrity principles.
Wemedoo supports clinical research globally and is trusted by customers across more than 25 countries.
Wemedoo AG is headquartered in Switzerland.
Wemedoo supports a wide range of organizations involved in clinical research and healthcare, including: Pharmaceutical and biotechnology companies, Medical device and MedTech companies, Food and cosmetics research organizations, Global and regional Contract Research Organizations (CROs), Hospitals and clinical research sites, Academic and research institutions.
Wemedoo supports clinical research organizations through a combination of advanced clinical technology and specialized operational expertise. Our services include: Protocol development, Clinical data management, Risk-based monitoring and source data review, eTMF setup and administration, Biostatistics and statistical programming, CDISC-compliant dataset generation, Medical writing and regulatory documentation.
Wemedoo is led by an experienced leadership team combining deep clinical expertise, technology innovation, and operational excellence: Nina Cihoric (Lic. oec./MSc) – Chief Executive Officer, Nikola Cihoric, MD – Founder and Chief Product Officer, Urosh Vilimanovich, PhD – Chief Customer Officer, Valérie Czaya, MA – Chief Operating Officer, Dusan Goljic, MPharm – Director of Quality Management.
