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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.

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.

Care without compromise: ensure vigilance through data

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Sectors

Pharma

Biotech

CRO

Medical device

Academia

Innovation at work

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Our success stories reveal how CRScube can transform your practice and clinical trial efficiency.

Featured case studies

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.

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.

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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