Where Safety, Clinical Trials,Â
and Real-World Data Connect
AB Cube Group unites clinical data management, structured oncology documentation, and regulatory safetyÂ
processes, supporting oncology research, pharmacovigilance workflows, and clinical studies across Europe.
The group brings together three complementary strengths. Its eClinical platform’s oncology trial expertise links with EHR cancer file and tumor board capabilities, connecting clinical trial data with structured real-world oncology care data. The pharmacovigilance solution completes the portfolio with safety and vigilance workflows, for one integrated approach across clinical trials, real-world data, and regulatory compliance.
Three Solutions, One Research Lifecycle
EHR Cancer Files and Tumor Board — Marvin
Tumor documentation, oncology registries, and multidisciplinary tumor boards — used by hospitals and academic institutions. Captures structured real-world oncology care data and connects it with clinical trial data.
Clinical Trial
Integrates clinical trial data into EHR cancer files and vice versa. Supports trial feasibility assessment and patient recruitment.
Real-World Data
Captures structured, longitudinal cancer patient data from routine clinical practice. Supports disease registries and long-term outcomes research.
eClinical Solution — Marvin
Clinical Trial
Manages the full clinical trial data lifecycle — eCRF design, query management, SDV, randomization, audit trails and CDISC compliance.
Real-World Data
Supports observational studies and long-term registries. Connects to EHR cancer files to reduce manual data entry and keep trial data current.
Patient Safety Solution — SafetyEasy®
Clinical Trial
Manages adverse event reporting within ongoing clinical studies. Automates SAE reconciliation, reducing manual effort by up to 70%.
Real-World Data
Enables post-market safety data collection and AI-based signal detection. Automates regulatory reporting (E2B, CIOMS) and literature surveillance.
AB CUBE GROUP IN NUMBERS
475+
Customers
20+
Years of Experience
800+
Active Sites
2,500+
Studies Conducted
Why AB Cube?
Adaptive & Complex Design Support
Configure umbrella, basket, platform and multi-arm trials. Handle multiple randomisations, sub-study branching, and mid-study protocol amendments without downtime.
CDISC-Native from the Ground Up
SDTM-based architecture end-to-end. Datasets are submission-ready from the start — no post-hoc mapping, no conversion effort.
Seamless Pharmacovigilance Integration
Bidirectional SAE reconciliation out-of-the-box. Automate case exchange between eClinical and PV, reducing manual effort by up to 70%.
AI-Powered Study Setup & CDISC Transformation
Automated eCRF generation from protocol documents, intelligent CDISC mapping, and AI-assisted study design. Reduce setup time from weeks to days.
Cost-Effective vs. Global Players
Enterprise-level functionality at a fraction of the cost. Oracle and Veeva are typically 3× more expensive with longer implementation cycles.
More Than 700 Trusted Oncology Sites
Sites know and trust Marvin across Europe — shortening onboarding and improving data quality from day one.
