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Trial team solutions

Seamless collaboration, one click at a time

Empowering trial teams to accelerate study timelines and enhance oversight with a comprehensive, interconnected platform.
Discover unparalleled efficiency and precision for all trial phases, no matter the complexity.

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A unified platform, widening possibilities

CRScube provides a central hub for orchestrating and monitoring clinical trials. With intuitive setup and easy amendments, a user-friendly suite of tools gives you full control of trial administration and learning, documentation, data management and risk-based monitoring.

Designed for actionable visibility

Our solutions deliver insights into critical data points, facilitating informed decision-making. By seamlessly integrating data within the platform, you manage trials more effectively and share a unified view of the truth. This reduces the need for data reconciliation, speeding up analysis and shortening time to trial results.

Products for trial teams

Experience seamless collaboration and accelerated study timelines with our interconnected solutions.

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The cornerstone of clinical data innovation

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Your clinical trial control tower

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Be inspection-ready… always

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Risk revelation: foresight at your fingertips

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Power up your team’s collective knowledge

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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

Features an intuitive user interface that simplifies navigation and operation for users, enhancing overall usability and efficiency.
Provides comprehensive manuals and libraries, supporting users with essential resources for effective task execution and problem resolution.
cubeCDMS is a reliable, validated system that complies with global standards and regulations.

Junseok P.

Manager Clinical Data Management

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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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Bio-Venture company achieves simple and robust imaging workflows with cubeCDMS

By implementing cubeCDMS, the sponsor successfully enabled Independent Radiological Review using raw DICOM files, ensuring unbiased and reliable endpoint evaluations.

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Implementing data-driven risk-based monitoring with cubeRBQM

For many years, CMIC relied on conventional methods – EDC, CTMS, and Excel trackers – to perform risk assessments.

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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.

See CRScube in action

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

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