Wemedoo oomnia EDC & RTSM

Wemedoo oomnia is the perfect fit for pharmaceutical companies, CROs, academia, medical device manufacturers, and visionaries aiming to advance in clinical research.

You can get EDC & RTSM as an independent tool or experience its full potential as part of the comprehensive and unified oomnia SaaS solution. It natively includes tools such as: Electronic Data Capture (EDC), Randomization & Trial Supply Management (RTSM), Clinical Trial Management System (CTMS), electronic Trial Master File (eTMF), electronic Patient Reported Outcomes (ePRO), electronic Clinical Outcome Assessment (eCOA), eConsent, and eSource. Access data and analytics across all tools, systems, and organizations in real-time.

Our Electronic Data Capture (EDC) tool is seamlessly integrated with RTSM, laboratory management, SAE report forms, protocol deviation logs, and more. It allows creation of any form type, providing strong data integration, personalized dashboards, and real-time reporting capabilities. These features collectively enable thorough oversight and efficient management of clinical trials. With its user-friendly configuration, controlled user access, and seamless data integration, Wemedoo oomnia EDC stands out as a premier solution in the industry.

The integrated Randomization and Trial Supply Management (RTSM) tool is equipped with comprehensive features that transform the processes of randomization, allocation to treatment, and trial supply management. As a component of our unified system, RTSM communicates automatically with other modules, enabling seamless randomization and treatment allocation directly within the electronic Case Report Form (eCRF).

- Customizable Data Capture: Create tailored forms with drag-and-drop simplicity, ensuring all necessary data is accurately collected.

- Automated Randomization & Supply Management: Simplifies trial operations by handling complex randomization and supply logistics in real-time.

- Integrated Ecosystem: Connect seamlessly with other clinical trial tools like RTSM, eTMF, and EHR systems for a unified workflow.

- Data Security & Compliance: Adheres to strict regulations with role-based access, encryption, and detailed audit trails.

- Data Evaluation & Reporting: Providing tools to generate reports and graphs that are useful for assessing study results in real-time.

- Enhanced Efficiency: Automates critical processes, reducing manual tasks and errors.

- Regulatory Compliance: Built-in compliance with industry standards like FDA 21 CFR Part 11.

- Scalability: Supports trials of any size, from small studies to global multi-site trials.

- Cost & Time Savings: Streamlined operations lead to faster trial completion and lower costs.

Wemedoo is your partner on your path to seamless clinical data management. Our solutions for sponsors, clinical research organizations, hospitals, and academia are built to effortlessly collect, analyze, and exchange clinical data in real-time. With our trusted expertise in clinical, medical, and real-world data interoperability, you can achieve significant improvements in data management and operational efficiency with solutions that are reliable, scalable, and tailored to your needs.

"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

"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." Dr. Georg Mathis, CEO Appeltree CI Group AG

If you are ready to enhance your clinical trial management with Wemedoo oomnia EDC & RTSM, click 'Get it now' in the top left corner or book a demo to begin your journey with oomnia EDC & RTSM.