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Trial team solutions

cubeRBQM

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Risk revelation: foresight at your fingertips

Stay ahead of potential issues with cubeRBQM – your comprehensive risk-based quality management solution for clinical trials. Gain unparalleled foresight, enabling your team to focus on what matters most: running a successful, compliant trial.

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Make smarter decisions with real-time insights

cubeRBQM gives study managers the tools to proactively identify and address risks. With real-time monitoring supported by intuitive dashboards, trial oversight becomes more streamlined and effective, so you can optimize your resources and reduce costly inefficiencies.

Streamlined risk management

Identify outliers and issues swiftly

Focus monitoring efforts on high-risk sites

Never miss a milestone with automated updates

Flexible data visualization

View centralized data from EDC, eSource, and wearable devices

Drill down into specific data points with ease

Share insights easily through downloadable reports

Simplify your workflow, amplify your impact

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Experience CRScube

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Intuitive setup, powerful integration

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cubeCDMS integration

Native integration with cubeCDMS for seamless data flow and navigation

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Dashboards

Pre-configured dashboards tailored to your study's needs

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Pre-validated views

Covering the most common monitoring requirements

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Additional views

Flexibility to add extra views based on protocol-specific needs

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Single sign-on

SSO for effortless transitions between systems

The CRScube difference

Developed by data managers

We understand your challenges because we've lived them

Continuous innovation

We're always pushing boundaries to serve you better

Data insights

We centralize your data to streamline analysis

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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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Improving the clinical data capture process with cubeDDC

The reliance on paper-based source documents and subsequent transcription into an Electronic Data Capture (EDC) system led to transcription errors, delayed data entry, and increased source data verification (SDV) costs.

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Efficiency by combining EDC and IRT

This European CRO’s decision to implement a combined approach with cubeCDMS and cubeIWRS provided them with an integrated, cost-effective, and innovative solution.

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Migrating to cubeCDMS to reduce costs and increase flexibility

This client leveraged cubeCDMS to reduce direct costs by an estimated 50-60% compared to their original EDC vendor.

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One-click randomization: confidence in every assignment

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See CRScube in action

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

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Get insights straight to your inbox

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The cornerstone of clinical data innovation

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One-click randomization: confidence in every assignment

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Experience the ease of automated updates

cubeRBQM keeps your data up to date, allowing your team to focus on improving trial quality without interruptions.

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