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Be inspection-ready… always

cubeTMF is your go-to platform for simplifying document management, ensuring compliance and maintaining smooth operations throughout your clinical trials.

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Complete oversight of your trial documentation

Our eTMF solution provides trial teams with a user-friendly platform for efficient management of trial master files. With real-time tracking and quality check processes, teams can ensure compliance across the lifecycle of their clinical trials.

Stay in control

Real-time notifications for overdue or missing files

Full audit trail for inspection readiness

Automated workflows for reviews and signatures

Enhanced efficiency

Batch uploads for faster document handling

Seamless collaboration between sponsors, CROs and sites

Instant access to essential trial documents

Simplify your workflow, amplify your impact

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Simplify your sites’ day-to-day operations

Managing Site Master Files (SMF) has never been easier. cubeTMF enables site staff to access, update and collaborate on documents in real-time, without the hassle of outdated and complex systems. Seamlessly connect sites and trial teams in one centralized platform, enhancing transparency and operational efficiency.

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Experience CRScube

Why choose our eTMF solution?

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Quality first

Enable quality checks and electronic signature processes, all fully traceable

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Fully compliant

Built to meet global regulatory requirements and compatible with the DIA TMF reference model

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Audit-ready

Quickly share relevant documents with auditors using a dedicated document storage area

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Adapted to your needs

Customize review and signature workflows to match your requirements

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Increased transparency

Visual indicators provide a quick overview of document status across your study

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Centralized monitoring

Check compliance with easy-to-track progress

Spend less time configuring your TMF

Set up new studies in no time by reusing existing binder structures.

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The CRScube difference

Developed with study managers

We carefully craft our solutions to address your challenges, simply

Continuous innovation

We’re always pushing boundaries to serve you better

Simple setup

Our solutions are easy to use and set up

The customer support team was incredibly responsive and helpful, addressing my questions promptly via email, and if needed, video call.

Joanne W.

Biomedical Engineer

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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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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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Reducing safety reporting budget by 80% with cubeSAFETY

A biotech company simplified their safety reporting, streamlined compliance and eliminated hidden fees.

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See CRScube in action

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

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Your clinical trial control tower

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The trusted formula for clarity and compliance

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