Trusted Partners
Trusted by Global Clinical
Research Teams
Trusted Partners
Our Platform
oomnia, our clinical research information system unifies clinical research and care, and turns fragmented data into a continuous, structured flow. It brings together eight essential tools as integrative parts of one unified system.
Real-Time. Adaptive. Seamless.
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Faster Trial Setup Client trial set up with 5000 questions compared to time needed by one of the biggest global CROs for the same trial in a different geography
Real-Time Trial Oversight
Client Retention
Tailored Solutions
Win more bids and execute trials faster. Eliminate complex integrations with a truly unified platform designed for rapid deployment.
Maintain 100% real-time oversight of your trial portfolio. Ensure data integrity, simplify compliance, and accelerate time to market.
Access an enterprise-grade clinical research system entirely for free. Unify your academic research with oomnia's academic license.
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
Society for Clinical Data Management
Wemedoo has been recognized by the Society for Clinical Data Management for innovation in clinical research — honored for our unified approach to clinical data management.
Trust & Security
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.
FDA 21 CFR Part 11
Compliant
GDPR
Compliant
HIPAA
Compliant
ICH GCP
Compliant
FAIR ALCOA+
Compliant
Swiss Data Privacy Law
Compliant
ISO 27001
Certified
ISO 9001
Certified
SOC 2
Certified
CDISC
Proud Member
Platform Results
Faster trial setup with unified architecture
Randomization & supply inside the eCRF
Real-time site inventory & trial status
Client retention rate
Artificial Intelligence
oomnia integrates powerful artificial intelligence to streamline complex processes, improve trial safety, and ensure you bring therapeutics to market faster and more efficiently.
Predictive analytics that identify risks early, enable scenario analysis, and dynamically adjust risk models throughout the trial lifecycle.
Real-time alerts with automated causality assessment and predictive modeling to enhance patient safety and accelerate response times.
Intelligent diversity profiling, bias detection, and recruitment strategy optimization to build representative, inclusive trial populations.
As members of EUCROF and ACDM, we are working together to raise the standards of clinical research and support the development of new approaches in the field.
Common Questions
Wemedoo clinical trial software is a unified clinical data management solution called oomnia that combines EDC, CTMS, eTMF, ePRO, eSource, eCOA, eConsent, and RTSM into one system. It is designed for CROs, sponsors, and academic researchers to manage clinical trials faster, with greater accuracy and full regulatory compliance.
oomnia includes eight integrated clinical trial software tools: Electronic Data Capture (EDC), Randomization and Trial Supply Management (RTSM), Electronic Trial Master File (eTMF), Electronic Patient-Reported Outcomes (ePRO), eSource for direct data capture, Electronic Clinical Outcome Assessment (eCOA), Electronic Informed Consent (eConsent), and Clinical Trial Management System (CTMS).
Wemedoo clinical trial software is used by Contract Research Organizations (CROs), pharmaceutical and biotech sponsors, and academic research institutions worldwide. It supports clinical trials of all phases and types, including medical device trials, decentralized trials, and real-world data studies.
Wemedoo's oomnia solution differentiates itself through true unification — all clinical trial tools operate from a single database, eliminating data reconciliation, reducing costs, and accelerating timelines. It won the SCDM Innovation Award 2025 for its unified approach to clinical data management.
Yes, Wemedoo clinical trial software is fully compliant with 21 CFR Part 11, HIPAA, GDPR, ICH GCP, and GxP requirements. The company is ISO 9001 and ISO 27001 certified, ensuring the highest standards of quality and data security.
