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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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Experience CRScube

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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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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A leading korean pharma optimized PV operations with cubeSAFETY

This leading pharmaceutical company transformed its pharmacovigilance operations by integrating cubeSAFETY with cubeCDMS.

See CRScube in action

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

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