An eCOA Platform Built for Oncology
Flexible, Cycle-Based Management Tailored to Your Trial
Revolutionize your oncology trials with our innovative eCOA platform designed to align with the unique needs of cancer research.
Our cycle-based management approach offers unparalleled flexibility, adapting to the nonlinear progression of oncology studies while ensuring optimal data quality and patient engagement. This purpose-built clinical trial tool streamlines workflows for sites, enhances the patient experience, and provides sponsors with real-time, actionable insights. In addition to supporting oncology research, this platform’s flexibility is ideal for any other therapeutic area that could benefit from a flexible, tailored eClinical solution.
Clinical Trial Engagement Made Simple
Empowering Patients
Our intuitive, patient-centric app transforms the clinical trial experience. By aligning with treatment cycles rather than rigid milestones, patients can easily track their progress and understand what to expect.
This approach reduces confusion, promotes active participation, and ultimately increases the accuracy of the data collected during the trial.
Streamlining Site Operations
Site staff benefit from our user-friendly interface that minimizes clicks and maximizes efficiency. Flexible scheduling accommodates unscheduled visits, dose adjustments, and treatment interruptions seamlessly.
By taking the guesswork out of patient management, our eClinical platform allows clinical teams to focus on what matters most: patient care and safety.
Enhancing Sponsor Oversight
Sponsors gain unprecedented visibility into trial progress with our comprehensive reporting tools. Our cycle-based approach enables more accurate monitoring of treatment responses, adverse events, and overall study timelines.
This data-driven insight allows for timely decision-making and more effective trial management.
Ensuring Data Quality and Compliance
Our eCOA system’s flexibility enhances data integrity. By allowing data collection to be tailored at both site and patient levels, we ensure that critical safety and efficacy measures are captured accurately, supporting robust analysis and regulatory compliance.
Personalized Implementation for Optimal Results
At Datacubed Health, we understand that every oncology trial is unique. That’s why we offer a fully configurable implementation process. Our team works closely with you to configure the platform to your specific protocol, ensuring that every aspect of the study is optimized for success.
From initial design to user acceptance testing, we provide end-to-end support, including:
- Protocol-specific configuration
- Integration with existing systems (EDC, IRT, sensors)
- Multilingual support for global trials
- Comprehensive training and technical support