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Pharmacovigilance

Safety mastery: turning data into insightful prevention

Weaving complex data into actionable safety insights – cubeSAFETY enables pharmacovigilance teams to track and report adverse events efficiently. Our automated, regulatory-compliant platform integrates seamlessly with other clinical data sources, ensuring thorough safety monitoring.

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You handle precision, we’ll handle compliance

Accurate reporting of adverse events is critical, so we continuously stay ahead of evolving global standards. With cubeSAFETY, your submissions are secure, accurate and always in line with regional expectations and the latest regulatory requirements. We help you get it right – first time.

Automation where you need it

cubeSAFETY eases your workload by streamlining case processing and automating key tasks. Pre-submission checks, facilitated agency communication and effortless integration with our EDC system make reporting smoother and more manageable.

Pharmacovigilance solutions

Discover more about our automated, regulatory-compliant system.

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Care without compromise: ensure vigilance through data

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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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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.

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Leveraging cubeCDMS planned SDV to improve monitoring efficiency

EPS adopted cubeCDMS Planned SDV as the foundation of its risk-based monitoring approach, enabling both the strategic and operational execution of risk-based monitoring.

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CRO improves study monitoring oversight and TMF completeness with cubeCTMS

By implementing cubeCTMS, the CRO aligned planning, reporting, and filing for monitoring in one reliable flow. Teams gained live visibility, reduced handoffs, and kept documentation current across countries and sites.

See CRScube in action

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

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