The trusted formula for clarity and compliance
Increase patient engagement and streamline the consent process with cubeCONSENT. Our electronic platform enhances patient understanding and compliance by increasing visibility of consent status, enabling faster decision-making and reducing delays in trial enrolment.
Patients deserve to understand your trial clearly
cubeCONSENT enhances a participant's awareness of a trial design and requirements and offers a personalized experience – leading to more positive patient engagement during the crucial enrolment phase.
Communicate differently
Interactive content platform
Multimedia capabilities
Break information into manageable pieces
Make it easy
Handheld-compatible
On-screen signature
Automated site notifications
Track enrolment, increase trial compliance
Simplify the informed consent form process, gaining real-time insights, and track updates effortlessly to ensure patients sign the correct version of the consent form.
Increase efficiency
Reduce paperwork
Eliminate manual tracking
Accelerate patient enrolment
Improve compliance
High data security
Adherence to regulatory standards
Comprehensive audit trail
Simplify your workflow, amplify your impact
The right solution for patients, sites and trial teams
Easy to use
Improve patient experience with our intuitive user interface
Portable
Patients and sites can access the ICF from anywhere, on any devices
Useful notifications
Sites know immediately when a patient has signed their ICF
Simpler management
Free up site staff to focus on participant care and trial management
Regulatory compliance
Meet local and global regulatory standards (FDA, EMA, HIPAA)
EDC integration
Remove the need for data reconciliation with seamless data flow to cubeCDMS
The CRScube Difference
Caring about patients
We offer tools that simplify patient participation in clinical trials
Continuous innovation
We’re always pushing boundaries to serve you better
Simple setup
Our solutions are easy to use and set up
Frequently asked questions (FAQs)
The customer support team was incredibly responsive and helpful, addressing my questions promptly via email, and if needed, video call.
Joanne W.
Biomedical Engineer
Featured case studies
Achieving rapid GCP compliance and seamless trial execution with cubeCDMS build support
Discover how JIHS used cubeCDMS and hands-on implementation support to build and launch a GCP-compliant EDC environment within just two months, while developing the internal expertise needed to support future double-blind clinical trials.
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