Better Data Quality. Better Research.
Marvin eClinical Suite:
Simplify your Clinical Trial
Empower your team to manage complex clinical trials and oncology data with integrated tools for cleaner, faster insights.
Built for every Organization from Academic Institutions to Biotech
Academic Institutions
What is Marvin?
Marvin is our robust, CDISC-certified EDC platform featuring a comprehensive suite of eClinical modules. Designed with end users in mind, Marvin simplifies clinical trial data management and supports efficient, high-quality research workflows.
Our oncology solutions (Marvin ODS and Marvin OTB) enable researchers to capture real-world oncology data through EHR-integrated cancer file and tumor board systems, thereby seamlessly connecting routine clinical care with clinical trial workflows.
Marvin EDC: Modules and Solutions for a smarter Trial
EDC/ eCRF
A powerful eClinical EDC platform built for complex oncology and cardiology trials. Fully configurable, CDISC-native, and AI-enabled.
ePRO
Collect Quality-of-Life or other real-world data directly from the patient – using predifened or own ePRO questionnairs.
RTSM
Advanced Patient Randomization and Enrollment
Marvin RTSM offers advanced randomization and material handling capabilities.
Safety
Handling Safety and Vigilance
Seamless integration between Marvin EDC and the SafetyEasy® Vigilance Suite enables faster, more efficient pharmacovigilance workflows.
Why Marvin & AB Cube?
Compliance & Security by Design - Built on a robust, pre-validated framework aligned with global regulatory standards and requirements.
Full Compliance with GCP and 21 CFR Part 11 Standards
Our solutions ensure full compliance with Good Clinical Practice (GCP) and are designed to meet the requirements of major regulatory bodies (FDA, EMA, MHRA, PMDA, etc.).
GDPR-Compliant Data Handling and EU Data Storage
We securely host data within the EU, ensuring GDPR compliance for European academic institutions while protecting sensitive patient data with SSL encryption and enterprise-grade security standards.
Secure Audit Trails and Role-Based Access Control
Maintain detailed audit trails for full transparency and enforce role-based access control to ensure that only authorized personnel can access or modify sensitive clinical data.
AB Cube handles the Complexity of Clinical Trials
Design Flexibility
Basket, umbrella, adaptive and platform designs within a standard configuration
Faster Set-Up with AI
AI-assisted eCRF creation from protocol, included edit checks and synthetic patients for testing
RTSM
Concurrent randomization across arms and cohorts without cross-system coordination.
Adaptive Protocols
Mid-study amendments via documented workflow with minimal disruption to sites.
Local lab
Unified lab ingestion for biomarker response data, audit-ready, no manual reconciliation.
ePRO & RBM
Improve data quality and trial efficiency with real-time patient insights and targeted monitoring
Built in Compliance
CDISC SDTM mapping embedded in study design, not post-collection, saving time during submission.
Ongoing data reconciliation
Embedded query workflow and safety data reconciliation between safety database and EDC
Real-time data cleaning
Inline edit checks and automated queries ensure high-quality data from the moment it is entered.
Faster Study Start-Up
Accelerate time from study design to first-patient-in using Marvin’s AI-enabled study build.
Lower Operational Risk
Unified data, quality controls, and automation reduce errors and operational oversights.
Accelerated Submission
Built-in compliance and reconciled data enable faster, first-time-right regulatory submissions.
Guiding You Through Every Step
Ranging from full-service support to a do-it-yourself approach, AB Cube allows you to select exactly the level of support you need.
Combine professional study setup, consulting, and training services to create the optimal setup for your organization.
Our Customer Success team is here to support you throughout your journey.
Trusted by Industry Leaders
Frequently Asked Questions
Answers to Help You
Make Decisions
What is Marvin EDC?
AB Cube Germany provides a solution called Marvin, a powerful EDC system for running clinical trials. We also offer powerful add-on modules such as ePRO and eConsent.
Is AB Cube Germany or Marvin a CRO?
No, AB Cube Germany is not a CRO. We are a dedicated provider of eClinical solutions such as EDC, ePRO, and eConsent. Our Customer Success team can support you in setting up your eCRF and eClinical solutions, but we are not a CRO. Through our extensive partner network, we can help you find CROs, data management providers, or other service partners.
Does Marvin EDC support all kind of Trials
Yes, Marvin EDC supports all phases and all study designs, including complex designs such as adaptive trial designs and randomized controlled trials (RCTs).
Is Marvin EDC hosted in a cloud?
Yes, Marvin is hosted in different data centers from two providers in Germany (Noris Network and Hetzner). Our data centers are certified according to ISO 27001, TÜVIT, and ISAE 3402.
Can I integrate Marvin with other systems?
Yes, we support integration rather than separation. Marvin is fully integrated into your eClinical solution architecture and supports various workflows.The integration works via APIs or our own Data Hub. Within the Data Hub, we have built-in integrations, such as the all-in-one vigilance solution SafetyEasy®.
Can I do SDTM tabulation with Marvin?
Yes, Marvin is 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.
Can I customize the system to fit my processes?
Absolutely. Marvin is fully modular and customizable and can be configured to fit your workflows.
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