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Patient-facing solutions

Empowering patients, illuminating outcomes

CRScube’s patient-centric tools empower study teams to improve participant engagement and data quality with intuitive mobile apps for electronic consent and patient-reported outcomes.

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Simple tools to enhance patient engagement

Striving to make the clinical trial journey as simple as it can be, we design tools that are easy to use.

Our electronic informed consent solution allows patients to read crucial information at their own pace, and our electronic patient-reported outcome (ePRO) reduces the burden for them by collecting data points remotely.

Not only does this make life easier for patients, but it also increases engagement and delivers data in real time – leading to greater accuracy and faster decisions.

Improve communication, minimize disruption

Patients who participate in clinical trials lead their everyday lives outside the trial setting, balancing personal, work, and family commitments.

To ensure they can seamlessly engage with the study, tools like ePRO and eConsent play a critical role – streamlining communication and allowing patients to provide timely feedback and consent without added burdens.

Patient-facing solutions

Discover tools designed with patient convenience in mind.

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Better patient data capture

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The trusted formula for clarity and compliance

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Experience CRScube

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Sectors

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Pharma

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Biotech

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CRO

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Medical device

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Academia

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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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Accelerating safety system adoption at a global pharma

In two weeks, CRScube's training and enablement gets PV teams up and running on cubeSAFETY.

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Linical unifies clinical trial documentation management with cubeTMF

To drive operational transformation, Linical implemented cubeTMF, a secure, GCP-compliant document management platform designed to centralize control while enabling global scalability.

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Improving case reporting by connecting cubeSAFETY with cubeCDMS

A mid-size biotech needed a safer and more efficient way to move adverse event data from their Electronic Data Capture (EDC) system into their safety database.

See CRScube in action

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

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