Care without compromise: ensure vigilance through data

cubeSAFETY empowers pharmacovigilance teams with an automated, compliance-first system, offering thorough safety monitoring and enabling meticulous attention to detail.

Submit with confidence, track with precision

Ensuring accurate reporting and regulatory compliance, cubeSAFETY simplifies case report submission and tracking.

Comprehensive safety management

Ensures regulatory compliance with ICH E2B and regional guidelines

Identifies safety signals from diverse data sources

Allows direct submission to FDA, EMA, CDE, MFDS, and PMDA using our dedicated gateways

Automatically translates entered data for CIOMS and XML submissions

Better processes

Provides real-time submission tracking

Prevents and manages duplicate case entries

Simplifies workflows with native AI features

Offers easy access to agency feedback

Simplify your workflow, amplify your impact

Experience CRScube

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Your ultimate safeguard for rigorous pharmacovigilance

AI-powered coding

Recommended medical coding terms and case narratives based on data input

Automated data entry

Import data from CIOMS PDF files with AI efficiency

Data transformation

Seamlessly import and export XML files and ICSR

Local & translated exports

Export raw or translated data as needed in multiple formats

cubeCDMS integration

Create cases with specific information, with bulk submission options

The CRScube difference

Developed by data managers

We understand your challenges because we've lived them

Continuous innovation

We're always pushing boundaries to serve you better

Loved by users

Our clients especially like the simple communication with regulatory agencies

CRScube strives to quickly resolve customer problems, lead clinical trends, and always strive to update the system on a regular basis!! It is structured to be easy to use for system users.

Yeonghwi L.

Database Administrator