Improving the clinical data capture process with cubeDDC

Efficiency by combining EDC and IRT

Migrating to cubeCDMS to reduce costs and increase flexibility

Reducing safety reporting budget by 80% with cubeSAFETY

Investigating high screening failure rates & data quality with cubeRBQM

Leveraging cubeRBQM to analyze adverse events trends

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Featured resources

Geekfest 2025 preparation journey by APAC director Uchiyama and manager Aono

We are pleased to host CRScube Geekfest 2025, our user conference in Japan, on Monday, June 16th, 2025, for pharmaceutical companies, CROs, and academia representatives who are currently using or considering implementing CRScube’s solutions.

Applying real world evidence to clinical trials with Cristina Chang

Cristina shares her deep insights into how real-world data is being applied to clinical trials to enhance patient outcomes, regulatory submissions, and post-marketing strategies.

"CRScube Geekfest 2025: Japan User Conference" Announcement

CRScube APAC is hosting its third annual Japan User Conference.

Innovation at work

CRScube helps trial teams, managers, sites, and safeguarding specialists realize outstanding efficiency to drive real-world impact.