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Patient-facing solutions

cubeCONSENT

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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.

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Our laser-focused determination turns visionary ideas into reality, propelling the clinical research industry forward.

The AI edge

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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

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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

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Simplify your workflow, amplify your impact

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Experience CRScube

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Our laser-focused determination turns visionary ideas into reality, propelling the clinical research industry forward.

The AI edge

The right solution for patients, sites and trial teams

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Easy to use

Improve patient experience with our intuitive user interface

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Portable

Patients and sites can access the ICF from anywhere, on any devices

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Useful notifications

Sites know immediately when a patient has signed their ICF

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Simpler management

Free up site staff to focus on participant care and trial management

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Regulatory compliance

Meet local and global regulatory standards (FDA, EMA, HIPAA)

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EDC integration

Remove the need for data reconciliation with seamless data flow to cubeCDMS

Keep tight control on ICF version

Easily update the Informed Consent Form, manage version tracking and notify sites about re-consenting requirements.

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 good thing about CRScube is that they listen carefully to user requests and quickly provide optimal solutions. It has helped me many times in the past during setup phase.

Hideyuki F.

Clinical Database Programmer

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Innovation at work

Our success stories reveal how CRScube can transform your practice and clinical trial efficiency.

Featured case studies

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Optimizing clinical trial setup through intelligent automation and cubeCDMS integration

Discover how SevenTwoOne, a CRO, uses AI, RPA, Microsoft Office, and cubeCDMS to transform EDC development, reducing manual effort across specification creation, test data generation, EDC builds, QC, and paper survey processing.

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Accelerating IVD and Medical Device Research

Efficiently managing complex study designs through modern clinical data management

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Practical innovation for better science: How CRScube internalized AI to accelerate innovation

By implementing AI in our own processes, we augment our capacity to innovate whilst maintaining the same quality level as our clients are used to.

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Related products

consent.webp

The cornerstone of clinical data innovation

consent.webp

Be inspection-ready… always

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Better patient data capture

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See CRScube in action

Explore how our platform will elevate your team and clinical trial management.

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